Biography
Dr. Momiao Xiong has earned various positions at different universities during his professional experience and currently Dr. Momiao Xiong is a Professor of Biostatistics at University of Texas School of Public Health, USA. Dr. Momiao Xiong is also an Adjunct Member of Graduate Faculty at Texas A&M University. Dr. Momiao Xiong has published various articles related to his field of interest in a variety of journal.
Research Interest
Dr. Momiao Xiong's research interests include:
Computational systems biology, functional genomics, bioinformatics, genetic epidemiology, statistical genetics, pharmacogenetics and population genetics
Related Publications
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Evolutionary Genetics Tracing the History of Life through DNA
Perspective:
DOI:
Lisa Ranford
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Post Translational and Conformational Changes in Proteins: Signal Transduction and Flagging
Commentary: Genet Disor Genet Rep
DOI:
Shall Laura
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Plants Utilized Against Bacterial and Mitigating Movement
Commentary: Genet Disor Genet Rep
DOI:
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Genetic Disorders and Their Inheritance Patterns
Short Communication:
DOI:
Virva Siira
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Gainful Plant-Related Microscopic Organisms and its Determination
Perspective: Genet Disor Genet Rep
DOI:
Andrew James
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Sub-atomic Hereditary Qualities of DNA Fix in Higher Plants
Perspective: Genet Disor Genet Rep
DOI:
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Genetic Engineering Ethics and Applications
Opinion Article:
DOI:
Amanda J
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Downsyndrome
Editorial: Genet Disor Genet Rep 2020
DOI:
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The Nature and Development of Plant Resistance
Opinion Article: Genet Disor Genet Rep
DOI:
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The Role of Chromosomes in Inheritance and Genetic Diversity
Opinion Article:
DOI:
Amine Bechar
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Pituitary Adenomas can cause Raised Degrees of Chemicals and Factors
Commentary: Genet Disor Genet Rep
DOI:
Carmen Payne
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Advancement of Basal-Cell Carcinoma or Cutaneous Cell Carcinoma
Commentary: Genet Disor Genet Rep
DOI:
Carla Berg
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Phenotypic Variances and Covariance into Genetic
Editorial: J Genet Disor Genet Rep
DOI:
Simon John
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Discoveries in Clear Cell Chondrosarcoma
Perspective: Genet Disor Genet Rep
DOI:
Michael Syam
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Adversely Affect Both Actual Wellness and Mental Turn of Events
Perspective: Genet Disor Genet Rep
DOI:
Sajeev Nair
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Lymphoblastic Cell Lines
Editorial: J Genet Disor Genet Rep
DOI:
Jobia Jolex
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Tissue Levels in Delicate Tissue Neoplasms
Opinion Article: Genet Disor Genet Rep
DOI:
Justin Mark
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Metabolic Syndrome X
Editorial: J Genet Disor Genet Rep
DOI:
Simiheer Khan
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Emerging Technologies in Genetic Testing and Screening
Perspective:
DOI:
Aileen Singh
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Evolutionary Genetic Information
Editorial: J Genet Disor Genet Rep
DOI:
Malika Qureshi
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Genetic Brain Disorders Complexities of the Human Mind
Perspective:
DOI:
Russell E Ware
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Removal of DNA Fragment
Editorial: J Genet Disor Genet Rep
DOI:
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Genomic Insights: Advances in Genetic Diagnosis and Therapeutic Strategies
Perspective:
DOI:
Shuang Kong
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Hereditary Tendencies: Genetic Disorders and their Association with Cancer
Commentary:
DOI:
Sarah Finning
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Genetic Epidemiology: Illuminating the Interplay between Genes and Disease
Commentary:
DOI:
Khaldar Safeukui
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Young Researchers Forum: Young Scientist Awards for System Biology 2020
Young Research Forum: J Genet Disor Genet Rep
DOI:
Gottfried Baier
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Market Analysis of Glycobiology and Glycochemistry 2020
Market Analysis: J Genet Disor Genet Rep
DOI:
Dr. Alireza Heidari
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Genetic Predisposition: Influence of Genetics on Disease Risk
Commentary:
DOI:
Yuin Hie
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Young Scientist Awards at Genome Editing 2020 for the best researches in Genome Editing and Gene Therapy
Young Research Forum: J Genet Disor Genet Rep
DOI:
William J. Rowe
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Human in Vitro Cellular Models
Editorial: J Genet Disor Genet Rep
DOI:
Chatchawan Jantasuriyarat
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Lymphoblastic Cell Lines
Commentary: J Genet Disor Genet Rep
DOI:
Stephanie Guseh
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Genetic Disorders and Therapeutic Interventions: Precision Medicine
Short Communication:
DOI:
Damon Salvatore
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Genetics of Neurological Disorders from Genes to Function
Opinion Article:
DOI:
Bokkers Bleiker
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Multifactorial and Polygenic Disorders: Unraveling the Complexity of Genetic Contributions
Opinion Article:
DOI:
Kasturi Haldar
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Understanding Genes and Chromosomes
Editorial: Genet Disor Genet Rep 2020
DOI:
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Metabolic Syndrome X
Commentary: J Genet Disor Genet Rep
DOI:
Simiheer Khan
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Unraveling Rare Genetic Variants and Their Clinical Implications
Opinion Article:
DOI:
Storgaard Nordestgaard
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Association Study of IVS8TGmTn Polymorphism and Cystic Fibrosis Disease in a Tunisian Population
Research Article: J Genet Disor Genet Rep, 6:1
DOI: 10.4172/2327-5790.1000147
Sahli Chaima, Hadj Fredj Sondess, Dabboubi Rym, Bousseta Khedija, Mehrzi Ahmed, Messaoud Taieb
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Congenital anomalies
Editorial: Genet Disor Genet Rep 2020
DOI:
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Neurocognitive Functioning in a Young Female with Weaver Syndrome
Case Report: J Genet Disor Genet Rep, 6:1
DOI: 10.4172/2327-5790.1000148
Wise JM, Cooper A, Crenshaw ML and Katzenstein JM
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Gene Card: A Personalized Guide to Genetic Counselling for Low Resource Countries
Research Article: J Genet Disor Genet Rep
DOI:
Anjali Aryamvally, Anwayee Das, Kriti Menon, Santhanam Rekha, Suman Jain, et al.
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Gene therapy
Editorial: Genet Disor Genet Rep 2020
DOI:
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Chromosome 22q11.2 and 7q11.23 Microdeletions in Children with Congenital Heart Defects Detected by Fish Technique
Research Article: J Genet Disor Genet Rep, 5:4
DOI: 10.4172/2327-5790.1000142
Mirea AM, Popp RA, Lazea C, Cuzmici Z, Al Khzouz C, Bucerzan S, Nascu, Man S, Iurian S, Miclea DL
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Glycobiology
Editorial: Genet Disor Genet Rep 2020
DOI:
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Young Scientist Awards at Genome Editing 2020 for the Best Researches in Genome Editing and Gene Therapy
Young Research Forum:
DOI:
William J. Rowe
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Evolutionary Genetic Information
Short Communication: J Genet Disor Genet Rep
DOI:
Malika Qureshi
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Evaluate RNA Sequences
Perspective: J Genet Disor Genet Rep
DOI:
Francesca Malchiodi
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Market Analysis of Genome Editing and Gene Therapy
Market Analysis: J Genet Disor Genet Rep
DOI:
William J. Rowe
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Aging: A Little (Oxidative) Stress is Good for You
Commentary: J Genet Disor Genet Rep
DOI:
Terrance J. Kubiseski
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A Case of MEN2A Associated with a C634R De-novo Mutation of the RET Gene at Algiers
Case Report: J Genet Disor Genet Rep
DOI:
Ammar Chikouche, Nadia Ould Bessi, Nawal Habak and Mebarek Boudissa
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Awards 2020 Genome Editing and Gene Therapy
Awards 2020: J Genet Disor Genet Rep
DOI:
William J. Rowe
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Evaluation of the Progression of Hybridoma Technology: Methods, Applications, Advantages and Drawbacks
Review Article: J Genet Disor Genet Rep
DOI:
Achim Cchitvsanzwhoh Satheka and Adhanom Mihretab Tesfamariam
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A Turner Patient Presenting Dicentric Ring X-Chromosome and Intellectual Disability
Research Article: J Genet Disor Genet Rep
DOI:
Bhavani G, Chandra R Samuel and Santhiya ST
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Novel Homozygous Variant of TBC1D8 Gene in Four Libyan Siblings with Autistic Spectrum Disorder and Intellectual Disability without Epilepsy
Research Article: J Genet Disor Genet Rep
DOI:
Adel Zeglam and Suad Alhmadi
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Fetuin A Concentration in the Amniotic Fluid of Fetuses with Down Syndrome
Research Article: J Genet Disor Genet Rep 2014, 4:1
DOI: 10.4172/2327-5790.1000118
Salih Burcin Kavak, Ebru Celik Kavak,Askin Sen, Rasit Ilhan, Murat Kaya, Ekrem Sapmaz, ozgur Arat, Sel?uk Kaplan and Melike Baspinar
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Single Amino Acid Deletion in MYH11 Segregating in a Family with TAAD
Case Report: J Genet Disor Genet Rep 2014, 4:1
DOI: 10.4172/2327-5790.1000119
Pawel T Pomianowski, Daniel Dykas, Murim Choi, Jingshing Wu, Gregory A Kuzmik, Dawn Ardito, Sandip Mukherjee and John A Elefteriades
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Mutations in the RB1 Gene in Argentine Retinoblastoma Patients and Uncommon Clinical Presentations
Research Article: J Genet Disor Genet Rep 2014, 4:1
DOI: 10.4172/2327-5790.1000120
Ottaviani Daniela, Parma Diana, Ferrer Marcela, Giliberto Florencia, Luce Leonela, Alonso Cristina and Szijan Irene
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Market Analysis of Glycobiology and Glycochemistry 2020
Market Analysis: J Genet Disor Genet Rep
DOI:
Alireza Heidari
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Impact of Consanguinity on Health in a Highly Endogamous Population in District Buner, Khyber Pakhtunkhwa, Pakistan
Research Article: J Genet Disor Genet Rep 2014, 4:1
DOI: 10.4172/2327-5790.1000121
Jehangir Khan, Arshad Ali, Bakht Tarin Khan , Zaheer Ahmad and Waqas Ahmad Shams
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Autosomal Dominant Inheritance: The Patterns of Genetic Transmission
Commentary: J Genet Disor Genet Rep
DOI:
Emily Bart
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Syndromic Autism Spectrum Disorder
Perspective: J Genet Disor Genet Rep
DOI:
Olivia Jhon
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Role of Genetic Factors and their Interaction in Life
Commentary: J Genet Disor Genet Rep
DOI:
Alex Ceron
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Cytogenetics: Exploring the Chromosomal Frontier of genome
Commentary: J Genet Disor Genet Rep
DOI:
Laura Hella
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Genetic Determinants of Salt- Sensitive Hypertension
Editorial: J Genet Disor Genet Rep 2012, 1:1
DOI: 10.4172/2327-5790.1000e101
Marlene Shehata, Fady Youssef and Alan Pater
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Chromosomal Disorders
Commentary: J Genet Disor Genet Rep
DOI:
Jobia Alex
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Genetic Basis of Phenotypic Variation: Exploring Individual Differences at the Molecular Level
Commentary: J Genet Disor Genet Rep
DOI:
Eli Bruce
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Genetic Studies of Complex Diseases in the Sequence Era
Editorial: J Genet Disor Genet Rep 2012, 1:1
DOI: 10.4172/2327-5790.1000e102
Momiao Xiong
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Chromosome Abnormalities and a Decreased Implantation Potential
Commentary: J Genet Disor Genet Rep
DOI:
Simon Alex
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Application of Laboratory Techniques for DNA and RNA Transformation
Perspective: J Genet Disor Genet Rep
DOI:
Luca Fronto
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Translational Research to Uncover Diagnostic & Therapeutic Gene Targets Emerging in a Genomic Era: from Bench to Bedside
Editorial: J Genet Disor Genet Rep 2012, 1:1
DOI: 10.4172/2327-5790.1000e103
Blum K, Giordano J, Borsten J, Downs BW, Hauser M, Simpatico T, Lohmann R, Braverman ER and Barh D
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Molecular Genetics: Unlocking the Perspective of Life
Perspective: J Genet Disor Genet Rep
DOI:
Cristina Palo
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Genetic Networks in Heterogeneous Populations
Editorial: J Genet Disor Genet Rep 2012, 1:1
DOI: 10.4172/2327-5790.1000e104
Mogen Fenger
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Modeling the Novel Gene in Zebra Fish: EXD2 (Exonuclease 3'-5' Domain Containing 2)
Research Article: J Genet Disor Genet Rep
DOI:
Shamsa Hilal Anzi, Hayfa Alrasheed, Maher M. Alsaif, Mohammed A. Aldahmesh
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Neurogenetics: The Intersection of Genetics and the Brain
Perspective: J Genet Disor Genet Rep
DOI:
Min Plenge
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Edwards Syndrome: A Genetic Disorder with Profound Impacts
Opinion Article: J Genet Disor Genet Rep
DOI:
Osaka Akiyama
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Genetic Development: The Process Behind Evolution of Gene Regulation
Opinion Article: J Genet Disor Genet Rep
DOI:
Jenny Hacken
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X Chromosomes Linked Traits: Unveiling the Genetics Chromosome
Short Communication: J Genet Disor Genet Rep
DOI:
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Endometriosis and Infertility
Special Issue Article: J Genit Syst Disord 2020
DOI:
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DNA Sequencing Methods
Perspective: J Genet Disor Genet Rep
DOI:
Arman Qureshi
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Gene Therapy for Mucopolysaccharidoses State of the Art
Perspective: Genet Disor Genet Rep
DOI:
Kitain Eric
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Endometriosis and Infertility
Special Issue Article: J Genit Syst Disord 2020
DOI:
Mohammad Ebrahim Parsanezhad
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Hematopoietic Stem Cell Gene Therapy Ameliorate Involvement
Perspective: Genet Disor Genet Rep
DOI:
Kevin Rock
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Genetic Disorders and Genetic Reports
Editorial: J Genet Disor Genet Rep
DOI:
Yanmin Yang
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Review on polycystic ovary syndrome, clinical manifestations, diagnostic
Special Issue Article: J Genit Syst Disord 2020
DOI:
Priyanga Poomani
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Development of Gene Therapies for Inborn Errors of Immunity
Commentary: Genet Disor Genet Rep
DOI:
Serdar Mohan
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Mutation: The Key to Our Evolution
Editorial: J Genet Disor Genet Rep
DOI:
Rajinder Kaul
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Assessing the current practice among doctors toward managing postpartum hemorrhage in Khartoum state 2018
Special Issue Article: J Genit Syst Disord 2020
DOI:
Rayan Adam Mahdi
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Homologous and Non Homologous End Joining
Opinion Article: J Genet Disor Genet Rep
DOI:
Arena Lac
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Externally Manufactured Investigational Cell-Gene Therapy Products
Commentary: Genet Disor Genet Rep
DOI:
Richard Kline
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Prevalence and correlates of female sexual dysfunctions- A pilotstudyfromBahrain
Special Issue Article: J Genit Syst Disord 2020
DOI:
Rizk Dee
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Clinical Hereditary Qualities Varies from Human Hereditary Qualities
Editorial: J Genet Disor Genet Rep
DOI:
Max Wilson
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Cell and Gene Therapies for Lung Diseases and Critical Illnesses
Opinion Article: Genet Disor Genet Rep
DOI:
Mathew Howard
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Human Umbilical Cord Tissue-Derived Mesenchymal Stem Cells and Stem Cell Condi- tioned Medium and their potentials towards regenerative application
Editorial: J Genit Syst Disord 2020
DOI:
Ranith Mishori
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Utilization of Customized Medication Incorporate Oncogenomics and Pharmacogenomics
Opinion Article: J Genet Disor Genet Rep
DOI:
Allen Stokes
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Transformations in Qualities on the X and Y Chromosome
Perspective: J Genet Disor Genet Rep
DOI:
Alex Hill
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Strategies for Non-Viral Quality Treatment
Perspective: J Genet Disor Genet Rep
DOI:
Kazuhiro Sakamoto
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Huge Scope Transformations in Chromosomal Design
Editorial: J Genet Disor Genet Rep
DOI:
Andy Crews
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Autosomal Predominant or Autosomal Passive are Utilized to Portray Quality Variations on Non Sex Chromosomes
Opinion Article: J Genet Disor Genet Rep
DOI:
Bell Hooks
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Pre-Implantation Genetic Diagnosis is the Hereditary Profiling of Undeveloped Organisms
Commentary: J Genet Disor Genet Rep
DOI:
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The Interpretation of Genetic Data - Considering the Effect of Changes to Gene Conformation - If the Facts Do not Support the Theory, Change the Theory-How Does This Contribute to Understanding Diabetes?
Commentary: J Genet Disor Genet Rep
DOI:
Graham Ewing
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Creature Hereditary Qualities Frequently Centers Around Parentage and Genealogy
Perspective: J Genet Disor Genet Rep
DOI:
David Axton
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Market Analysis of Genome Editing and Gene Therapy
Market Analysis: J Genet Disor Genet Rep
DOI:
William J. Rowe
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Genotype is Alluded to as Heterozygous
Editorial: J Genet Disor Genet Rep
DOI:
Aaron Wolfe
-
Cytogenetic is Basically a Part of Hereditary Qualities
Editorial: J Genet Disor Genet Rep
DOI:
Bell Jones
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Advancement in Gene Therapy and Genome Editing
Editorial: J Genet Disor Genet Rep
DOI:
Yanmin Yang
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Undiagnosed/Untreated Phenylketonuria (PKU) With Normal IQ and the Possible Role of Magnetic Resonance Spectroscopy (MRS)/Correlated Spectroscopy (COSY)
Review Article: J Genet Disor Genet Rep
DOI:
William B Hanley*
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Advancements in Genomic Sequencing Technologies: Implications for Genetic Diagnosis
Commentary: J Genet Disor Genet Rep
DOI:
Laura Hailden
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Apert Syndrome: A Comprehensive Examination of Craniosynostosis and Limb Abnormalities
Short Communication: J Genet Disor Genet Rep
DOI:
Anna Monti
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Understanding Thalassemia and Hemoglobinopathies: Insights and Implications
Commentary: J Genet Disor Genet Rep
DOI:
Rico Samuel
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Gene Therapy for Inherited Genetic Disorders: Recent Breakthroughs and Challenges
Commentary: J Genet Disor Genet Rep
DOI:
Jiayi Kevin
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CGH Array Based Case Report of a Patient Suffering with Amelogenesis Imperfecta, Jalili Syndrome, Situs Inversus and Oligozoospermia
Research Article: J Genet Disor Genet Rep
DOI: 10.4172/2327-5790.1000122
Neetu Singh, Dinesh Kumar Sahu, Parth Purwar, Sanjeev Gupta, Anil Kumar Tripathi, Jaya Dixit, Ravi Kant and Devendra Kumar Gupta
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Endovascular Treatment of Lower Extremity Venous Insufficiency
Commentary: J Genet Disor Genet Rep
DOI:
Steven Parks*
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Global Initiatives in Genomic Medicine: Collaborative Approaches to Treat Genetic Disorders
Perspective: J Genet Disor Genet Rep
DOI:
Amy Chen
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Patau's Syndrome: A Comprehensive Exploration of a Complex Genetic Disorder
Perspective: J Genet Disor Genet Rep
DOI:
Tae Zhenag
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Understanding Congenital Adrenal Hyperplasia: Genetic and Hormonal Complexities Unveiled
Perspective: J Genet Disor Genet Rep
DOI:
Patrica Licio
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Postoperative Sickness and Heaving: Understanding the Mystery
Commentary: J Genet Disor Genet Rep
DOI:
George Volkert*
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Ehlers-Danlos Syndrome: Subtypes and Diagnostic Advances Explored
Opinion Article: J Genet Disor Genet Rep
DOI:
Eric Romano
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Chromosomal Shakiness and Aneuploidy as Reasons for Disease Drug Obstruction
Opinion Article: J Genet Disor Genet Rep
DOI:
Maeve M Monkaaa*
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Precision Medicine in Genetic Disorders: Current State and Future Prospects
Opinion Article: J Genet Disor Genet Rep
DOI:
Cindy Hiwai
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Demystifying Marfan Syndrome: Insights into Genetic Origins and Clinical Features
Opinion Article: J Genet Disor Genet Rep
DOI:
Alissa Paul
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RPOB Gene Polymorphism and its Association with Multi Drug Resistance Pattern of Mycobacterium Tuberculosis and Associated Risk Factors among TB Patients
Research Article: J Genet Disor Genet Rep, 4:2
DOI: 10.4172/2327-5790.1000123
Tekeba Sisay and Nega Berhane
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Ring14 International:Development of a National-Based Patient Association towards a âGlobalâ Network Initiative to Fight a Chromosomal Disorder
Short Communication: J Genet Disor Genet Rep, 4:2
DOI: 10.4172/2327-5790.1000124
Stefania Azzali, Yssa DeWoody, Berardo Rinaldi and Marco Crimi
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Ring 9 Chromosome Syndrome in Black African Infant
Case Report: J Genet Disor Genet Rep, 4:2
DOI: 10.4172/2327-5790.1000125
Alao MJ, Lal�y� A, Adjagba M, Ayivi B and Darboux R
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Indigenous Complimentary Health Seeking Behavior among Caregivers of Sickle Cell Disorder in Nigeria
Research Article: J Genet Disor Genet Rep, 4:2
DOI: 10.4172/2327-5790.1000126
Omiunu Ojinga Gideon and Akahchukwu Patience Chioma
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Market Analysis of Glycobiology and Glycochemistry 2020
Market Analysis: J Genet Disor Genet Rep
DOI:
Dr. Alireza Heidari
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Genetic Predisposition and Environment Factors
Editorial: Genet Disor Genet Rep
DOI:
Bob Mareley
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Young Researchers Forum: Young Scientist Awards for System Biology 2020
Young Research Forum: J Genet Disor Genet Rep
DOI:
Gottfried Baier
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Comparison of Sire Component Estimates Between Male and Female Offspring.
Editorial: Genet Disor Genet Rep
DOI:
Nobuo Kanazawa
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Neoplasia Caused by Asbestos Exposure
Editorial: Genet Disor Genet Rep
DOI:
Bob Mareley
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Aging: A Little (Oxidative) Stress is Good for You
Commentary: J Genet Disor Genet Rep
DOI:
Terrance J. Kubisesk
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Mental Illnesses
Editorial: Genet Disor Genet Rep
DOI:
Basin Mahar
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The Inside and out Assessment of Thought Mitochondrial Sickness
Commentary: J Genet Disor Genet Rep
DOI:
Roger Federer*
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Abnormalities in Human Embryos
Editorial: Genet Disor Genet Rep
DOI:
Basin Mahar
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Changes in GNRH1 as an Uncommon Reason for Separated Inadequacy
Commentary: J Genet Disor Genet Rep
DOI:
Root Willson*
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A Hereditary Calculation Adjustment Technique in Light of Intermingling
Opinion Article: J Genet Disor Genet Rep
DOI:
Woakes Chris*
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Preimplantation Hereditary Testing: An Audit of Current Modalities
Opinion Article: J Genet Disor Genet Rep
DOI:
Williamson Kristen*
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Effect and Co-operations among Smoking and Customary Prognostic Elements
Perspective: J Genet Disor Genet Rep
DOI:
Jordan Kate*
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Young Scientist Awards at Genome Editing 2020 for the best researches in Genome Editing and Gene Therapy
Young Research Forum: J Genet Disor Genet Rep
DOI:
William J. Rowe
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Mutation: The Key to Our Evolution
Editorial: J Genet Disor Genet Rep
DOI:
Rajinder Kaul
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Conceptual of Autism
Editorial: Genet Disor Genet Rep 2020
DOI:
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Bioinformatics
Editorial: Genet Disor Genet Rep 2020
DOI:
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Genetic Brain Disorders
Editorial: Genet Disor Genet Rep 2020
DOI:
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DNA: Desoxyribonucleic Acid
Editorial: Genet Disor Genet Rep 2020
DOI:
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Genetic Epidemiology
Editorial: Genet Disor Genet Rep 2020
DOI:
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Young Researchers Forum: Young Scientist Awards for Genetics 2020
Young Research Forum: J Genet Disor Genet Rep
DOI:
Gail Risbridge
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Young Researchers Forum: Young Scientist Awards for System Biology 2020
Young Research Forum: J Genet Disor Genet Rep
DOI:
Gottfried Baier
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History Versus Limits of Science: Is Solomonic Genius a Y Chromosome Phenomenon?
Rapid Communication: J Genet Disor Genet Rep 2014, 3:2
DOI: 10.4172/2327-5790.1000114
F I D Konotey-Ahulu
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Maternal and Paternal Age at Pregnancy for Low Incidence Trisomy Groups: Preliminary Findings and Implications
Research Article: J Genet Disor Genet Rep 2014, 3:2
DOI: 10.4172/2327-5790.1000115
Katherine S Ancell and Deborah A Bruns
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Cross-Sectional Cohort Ukrainian Megapolice Sample Study of People�s Reactions to Faces of Patients with Different Mental Conditions
Research Article: J Genet Disor Genet Rep 2014, 3:2
DOI: 10.4172/2327-5790.1000116
Filiptsova OV and Atramentova LA
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Biotinidase Deficiency Presenting as Hyperventilation Syndrome
Case Report: J Genet Disor Genet Rep, 6:1
DOI: 10.4172/2327-5790.1000149
Iwanicka-Pronicka K, Pajdowska M, Dariusz Rokicki, Piekutowska-Abramczuk D, Kozlowski D,Wisniewska-Ligier D, Ksiazyk JB, Krajewska-Walasek M, Wolf B and Pronicka E
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PROK2 and PNCK â Novel Proteins Present in Follicular Fluid of Mature and Immature Human Oocytes: Preliminary Study
Research Article: J Genet Disor Genet Rep, 6:1
DOI: 10.4172/2327-5790.1000150
Burnik Papler T, Verdenik I, Devjak R,Vrtacnik Bokal E
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Ethical Implications in Genetic Counseling and Family Studies of the Epilepsies
Editorial: J Genet Disor Genet Rep
DOI:
Béatrice Godard
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Glucocorticoids are among the Best Treatments in the Therapy of Persistent Incendiary and Immune System Illnesses
Commentary: J Genet Disor Genet Rep
DOI:
Behzad Behnam
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Perceptions of Genetic Discrimination among at Risk Relatives of Colorectal Cancer Patients
Perspective: J Genet Disor Genet Rep
DOI:
Sakshi Kaur
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Novel Mutation in Slc37a4 Gene Found by Whole-Exome Sequencing in Type I Glycogen Storage Disease (Von Gierke)
Research Article: J Genet Disor Genet Rep
DOI:
Zakieh Siahpoosh
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Genetics 2020- Market Analysis
Market Analysis: J Genet Disor Genet Rep
DOI:
VINCENT STEVEN
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Identification of a Novel Mutation in the Human ARSB Gene on Chromosome 5q14.1 for Autosomal Recessive Mucopolysaccharidosis Type VI Patients in Southwest Colombia
Case Report: J Genet Disor Genet Rep, 6:1
DOI: 10.4172/2327-5790.1000151
Acosta MA, Lago RM,Barros F,Carracedo AM
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Penile Sebaceous Adenoma with Sporadic Loss of MLH-1 and PMS2 Protein Expression: A Case Report and Review of Literature
Case Report: J Genet Disor Genet Rep
DOI:
Blaire A. Anderson, Shaofeng Yan and Bing Ren
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Understanding the Genetic Basis, Clinical Manifestations, and Therapeutic Approaches for Congenital Adrenal Hyperplasia
Commentary: J Genet Disor Genet Rep
DOI:
Farid Ahmed
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X-Linked Inheritance and Dominance: Clinical Insights and Management Strategies
Perspective: J Genet Disor Genet Rep
DOI:
Mich González
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Market Analysis of Genome Editing and Gene Therapy
Market Analysis: J Genet Disor Genet Rep
DOI:
William J. Rowe
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Genetic Reports in Population Health: Current Trends and Implications
Opinion Article: J Genet Disor Genet Rep
DOI:
Nasser Khan
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Integrative Genomics Approaches Unraveling the Complexity of Uncommon Genetic Disorders
Opinion Article: J Genet Disor Genet Rep
DOI:
Dalton Smith
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The Genomic Renaissance: A Comprehensive Overview of Emerging Technologies in Genetic Diagnosis
Commentary: J Genet Disor Genet Rep
DOI:
Sean Adrian
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International Conference on Genetic Mutations and Disorders
Editorial: J Genet Disor Genet Rep
DOI:
RAUSCHER ALEXANDER
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Young Scientist Awards at Genome Editing 2020 for the best researches in Genome Editing and Gene Therapy
Young Research Forum: J Genet Disor Genet Rep
DOI:
William J. Rowe
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Young Research Forum-Young Scientist Awards at Glycobiology 2020
Young Research Forum: J Genet Disor Genet Rep
DOI:
Alireza Heidari
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Execution of a Cutting Edge Sequencing Test for Checking of Blended Chimerism
Opinion Article: Genet Disor Genet Rep
DOI:
Dan Hauzenberger*
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Molecular Genetic Testing for Carrier - Prenatal Diagnosis and Computational Analysis of Oculocutaneous Albinism Type 1
Research Article: J Genet Disor Genet Rep 2014, 3:2
DOI: 10.4172/2327-5790.1000117
Kathirvel Renugadevi, John Asnet Mary, Vijayalakshmi Perumalsamy, Suresh Seshadri, Sujatha Jagadeesh, Beena Suresh, Sheela Nampoothiri, Rajaiah Shenbagarathai, Sankaran Krishnaswamy and Periasamy Sundaresan
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Molecular characterization of Galactosemia in Iran: identification of Eleven mutations.
Research Article: J Genet Disor Genet Rep
DOI:
Mehrnoosh Moody
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Peutz-Jeghers Syndrome: Current State-of-the-Art.
Review Article: J Genet Disor Genet Rep
DOI:
Cipta Mahendra
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Endometrial Disease in Adults
Opinion Article: J Genet Disor Genet Rep
DOI:
Thomas Aldy
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Torment can be available in the Perineum
Perspective: J Genet Disor Genet Rep
DOI:
David Farooq
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Drawn out Pregnancy is Related with an Increment in Perinatal Horribleness during Child Birth
Opinion Article: J Genet Disor Genet Rep
DOI:
Laura Lewis
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How Menopause Causes Health Issues in Women after Pregnency
Commentary: J Genet Disor Genet Rep
DOI:
Lambrinoudaki Caty
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Thyroid Issues can be Difficult to Analyze in Pregnancy
Perspective: J Genet Disor Genet Rep
DOI:
Chan Li
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Chromosomal Abnormalities: Causes and Effects on Development
Perspective:
DOI:
Mustafa Gokhan Ertosun
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A Rare Familial Paracentric Inversion in the Long Arm of Chromosome 8: Case Report and Review of the Literature
Research Article: J Genet Disor Genet Rep, 6:2
DOI: 10.4172/2327-5790.1000152
Kouvidi E, Tsarouha H, Zachaki S, Mitrakos A, Sfakianoudis K, Kanavakis E, Mavrou A
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Homozygous Point Mutation in a Patient with Spinal Muscular Atrophy Type 1
Case Report: J Genet Disor Genet Rep 2016, 5:3
DOI: 10.4172/2327-5790.1000137
Isa Abdi Rad, Ali Vahabi and Ahad Ghazavi
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Investigation of the Origin of Common LDLR Mutation Alleles in New Zealand Familial Hypercholesterolemia Patients
Research Article: J Genet Disor Genet Rep, 7:1
DOI: 10.4172/2327-5790.1000167
Laurie AD, Spain RJ, Reid N and George PM
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Challenging Reproductive Genetic Counseling in Families at High Risk for Rare Genetic Syndromes â A Case Report with Possible Denys-Drash Syndrome
Case Report: J Genet Disor Genet Rep, 7:2
DOI: 10.4172/2327-5790.1000172
Hachmeriyan M, Andonova S, Levkova M, Stoyanova M, Kalchev K, Vasilev P, Miteva V, Tsvetkova M, Bradinova I and Angelova L
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Severe Expressive-Language Delay and Congenital Malformations in a Boy with Microduplication 7q11.23 Diagnosed by Molecular Cytogenetic Analysis
Research Article: J Genet Disor Genet Rep 2016, 5:1
DOI: 10.4172/2327-5790.1000127
Inesse Ben-Abdallah-Bouhjar, Amal Al Hashem, Samia Sobki, Brahim Tabarki, Yasser Hassen Babair and Hatem Elghezal
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Mutational Analysis in Gaucher Disease: Implications in Genetic Counseling and Management.
Research Article: J Genet Disor Genet Rep 2016, 5:2
DOI: 10.4172/2327-5790.1000132
Inusha Panigrahi, Jaswinder Kalra, Prasoon Goyad, Preeti Khetarpal and Anjana Munshi
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Treatment with Agalsidase Alfa during Pregnancy in a Heterozygous Female with Fabry Disease
Case Report: J Genet Disor Genet Rep, 5:4
DOI: 10.4172/2327-5790.1000143
Antonio Pisani, Giuseppe Bifulco, Attilio Di Spiezio Sardo and Eleonora Riccio
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A Rett Syndrome Case with Mutation in MECP2 and Deletion of 16p11.2
Case Report: J Genet Disor Genet Rep, 6:3
DOI: 10.4172/2327-5790.1000158
Bossolani-Martins AL, Moreira DP, Lourenço NCV, Magalhaes ML, Ribeiro CM, Griesi-Oliveira K and Fett-Conte AC
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Intergenerational De Novo Spinocerebellar Ataxia 7 CAG Enlargement in a Moroccan Family Detected by Triplet Primed PCR
Research Article: J Genet Disor Genet Rep, 6:4
DOI: 10.4172/2327-5790.1000163
Martínez-Laso J, Giménez-Pardo A Jimenez E, Gallego J, Cervera I, Ayuso C, Lorda I and Trujillo-Tiebas MJ
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Evidence that lithium Inhibits Export of N-Acetyl-L-Aspartate from Neurons: A Retrospective Study of Canavan Disease and Bipolar Disorder Patients
Research Article: J Genet Disor Genet Rep 2014, 3:1
DOI: 10.4172/2327-5790.1000110
Morris H Baslow and David N Guilfoyle
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Hereditary Thrombocytosis in 3 Kuwaiti Siblings with Homozygous MPL Pro106Leu Mutation and Abnormal Platelet Aggregation
Case Report: J Genet Disor Genet Rep 2013, 2:2
DOI: 10.4172/2327-5790.1000105
Preethi Reddy Marri, Salman Kirmani and Vilmarie Rodriguez
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Whole Exome Sequencing found a Novel Truncating Mutation within CNTNAP2 Gene in an Iranian Patient with Mental Retardation
Case Report: J Genet Disor Genet Rep, 7:3
DOI: 10.4172/2327-5790.1000177
Mehrnoosh Shokoohi, Mohammadreza Hajjari, Javad Mohammadiasl J and Maryam Tahmasebi Birgani MT
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Inherited Unbalanced Chromosome from Parent with Balanced Translocation: A Case Report and Review of Literature
Case Report: J Genet Disor Genet Rep 2016, 5:3
DOI: 10.4172/2327-5790.1000138
Kumari P, Mishra VV and Tewari S
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TLR4 and NOD2/CARD15 Polymorphisms and Their Association with Dietary Factors in Colorectal Cancer
Research Article: J Genet Disor Genet Rep, 7:1
DOI: 10.4172/2327-5790.1000168
Omrane I, Baroudi O, Medimegh I, Ayari H, Kourda N, Mezlini A and Benammar-Elgaaied A
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Phenylketonuria and Genetics
Review Article: J Genet Disor Genet Rep, 7:2
DOI: 10.4172/2327-5790.1000173
Ittan SP
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Screening of Genetic Mutations in GBA1, GIGYF2 and VPS35 in Parkinson Disease Patients from India
Research Article: J Genet Disor Genet Rep, 5:4
DOI: 10.4172/2327-5790.1000144
Tamali Halder, Janak Raj, Sharad Pandey, Ajay Kumar, Sagar Kawale, Sandeep Chaudhary, Vivek Sharma, Deepika Joshi and Parimal Das
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The Genomic Novel and Priority Mapping Tool: Using Empathic Design to Develop Innovative Patient-Centered Decision-Making Tools for the Genomic Testing Experience
Research Article: J Genet Disor Genet Rep 2016, 5:1
DOI: 10.4172/2327-5790.1000128
Kiley J Johnson, Kimberly A Schahl, Pamela S Sinicrope, Tammy M McAllister, Jennifer B McCormick, Leslie E Ruckman, Mekayla I Beaver and Noralane M Lindor
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Comprehensive Review of Rare Hereditary Autoinflammatory Disorders
Review Article: J Genet Disor Genet Rep 2013, 2:2
DOI: 10.4172/2327-5790.1000106
Nobuo Kanazawa
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The Interpretation of Genetic Data - Considering the Effect of Changes to Gene Conformation - If the Facts Donât Support the Theory, Change the Theory â How Does This Contribute to Understanding Diabetes?
Commentary: J Genet Disor Genet Rep, 6:4
DOI: 10.4172/2327-5790.1000164
Ewing GW
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Cerebellar Hypoplasıa as a Manıfestatıon of 6q25 Deletıon in a Preterm Newborn
Case Report: J Genet Disor Genet Rep, 7:3
DOI: 10.4172/2327-5790.1000178
Demırel G, Vatansever B, Karavar H, Gundogdu S, Ertan G and Tastekın A
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Resistance of Culex pipiens (Diptera: Culicidae) to Chlorpyrifos Insecticide in Central Tunisia
Research Article: J Genet Disor Genet Rep, 6:3
DOI: 10.4172/2327-5790.1000159
Jaber Daaboub, Ahmed Tabbabi, Raja Ben Cheikh, Ali Lamari, Ibtissem Ben Jha and Hassen Ben Cheikh
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Growth Abnormalities Resulting in Short Stature in Genetic Syndromes
Review Article: J Genet Disor Genet Rep 2014, 3:1
DOI: 10.4172/2327-5790.1000111
Lena Dain1 and Stavit A Shalev
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Pallister-Killian Syndrome: Undetected by Percutaneous Umbilical Blood Karyotyping and Neonatal Blood Microarray Comparative Genomic Hybridization
Research Article: J Genet Disor Genet Rep, 6:2
DOI: 10.4172/2327-5790.1000153
Huang MH, Yang IF, Lee C, Chang JS, Wang HC, Tou WS, Ling FC, Lai HL, Tsai LP and Ho SP
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A Case of Wolf-Hirschhorn Syndrome and Familial Mediterranean Fever
Case Report: J Genet Disor Genet Rep 2016, 5:2
DOI: 10.4172/2327-5790.1000133
Kazuaki Matsumoto* and Masayasu Ohta
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A case of Tuberous Sclerosis Complex Masquerading as Birt-Hogg-Dubé Syndrome
Case Report: J Genet Disor Genet Rep, 7:1
DOI: 10.4172/2327-5790.1000169
Kong YL, Oon HH, Choudhury Y, Tan MH and Ng SK
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A Rare Case of Isodicentric Xq28 that Causes Mental Retardation: Molecular Characterization and Review
Research Article: J Genet Disor Genet Rep, 6:2
DOI: 10.4172/2327-5790.1000154
Gonzalez C, Gutierrez M, Ruiz ML, Huete B, Gonzalez S, Gallego J and Cava F
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Are Antimullerian Hormone and its Receptor Genes Associated with Low Ovarian Response?
Research Article: J Genet Disor Genet Rep 2014, 3:1
DOI: 10.4172/2327-5790.1000112
Chelsi Goodman, Hosam Zaki, Larry Fischel, Hisham Greiss and Carolyn Coulam
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Evaluation of Genomic Evidence for Oxidative Stress in Experimental Radiation Nephropathy
Research Article: J Genet Disor Genet Rep 2013, 2:1
DOI: 10.4172/2327-5790.1000101
Eric P Cohen, Marek Lenarczyk, Brian L Fish, Shuang Jia, Martin J Hessner and John E Moulder
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Left Ventricular Noncompaction in Noonan Syndrome
Case Report: J Genet Disor Genet Rep 2016, 5:2
DOI: 10.4172/2327-5790.1000134
Robert B Hinton, Paula Goldenberg, Richard C Godby, Ashley Parrott, Amy G Shikany, Benjamin J Landis, Jeanne F James, Erin M Miller, Stephanie M Ware
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Hearing in Williams Syndrome: From Input to Processing
Review Article: J Genet Disor Genet Rep, 7:2
DOI: 10.4172/2327-5790.1000174
Fagundes Silva LA, Kim CA and Matas CG
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Anti-Ige (Omalizumab) Improved Trombotic Emboli by Elevating Activated Protein C, Protein S, and Antithrombin III in a Case of Prothrombin G20210A Mutation: Long Term Follow-Up
Letter to Editor: J Genet Disor Genet Rep 2016, 5:1
DOI: 10.4172/2327-5790.1000129
Arzu Didem Yalcin and Betul Celik
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Congenital Cerebral Ischemic Lesions in Monochorionic Twins
Case Report: J Genet Disor Genet Rep 2013, 2:2
DOI: 10.4172/2327-5790.1000107
Olajide Dolapo and Ravi Kudumula
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Rare Unusual Coincidence of LeriâWeill Dyschondrosteosis Resulting from a Downstream Enhancer Deletion of SHOX Gene and Neurofibromatosis Type 1
Case Report: J Genet Disor Genet Rep, 6:4
DOI: 10.4172/2327-5790.1000165
Peleg A, Adir V, Larom-Khan G, Harari Shaham A and Sagi-Dain L
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Clinical and Molecular Assessment in a Female with Fragile X Syndrome and Tuberous Sclerosis
Research Article: J Genet Disor Genet Rep 2016, 5:3
DOI: 10.4172/2327-5790.1000139
Carolyn M Yrigollen, Laura Pacini, Veronica Nobile, Reymundo Lozano, Randi J Hagerman, Claudia Bagni and Flora Tassone
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Smith-Magenis Syndrome Treated with Ramelteon and Amphetamine-dextroamphetamine: Case Report and Review of the Literature
Case Report: J Genet Disor Genet Rep, 5:4
DOI: 10.4172/2327-5790.1000145
Baek WS, Elsea SH
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Non-Viral Vectors for Cystic Fibrosis Therapy: Recent Advances
Review Article: J Genet Disor Genet Rep, 7:3
DOI: 10.4172/2327-5790.1000179
Faisal Qaisar, Anum Habib, Noor Muhammad and Zia ur Rehman
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A New Case of Microdeletion 5q11.2 with Segmental 5q Isodisomy and Review of the Literature
Case Report: J Genet Disor Genet Rep, 6:3
DOI: 10.4172/2327-5790.1000160
Pecile V, Devescovi R, Cappellani S, Faletra F and Lenzini E
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Long-Term Follow-Up of a Patient with Sitosterolemia and Hemolytic Anemia with Excellent Response to Ezetimibe
Case Report: J Genet Disor Genet Rep 2013, 2:1
DOI: 10.4172/2327-5790.1000102
Alfonso Quint?s-Cardama and John J. McCarthy
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Same Mutation in Two Patients with Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome) Coming from Different Municipalities in the Department of Cauca, Southwestern Colombia
Research Article: J Genet Disor Genet Rep, 5:4
DOI: 10.4172/2327-5790.1000146
Acosta MA, Lago RM, Barros F and Carracedo AM
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Lipoprotein Glomerulopathy: Molecular Characterization of Three Italian Patients and Literature Survey
Research Article: J Genet Disor Genet Rep 2014, 3:1
DOI: 10.4172/2327-5790.1000113
Antonio Pasquariello, Livia Pisciotta, Tiziana Sampietro, Giovanna Pasquariello, Pellegrino Masiello, Matilde Masini, Francesco Sbrana, Mariarita Puntoni, Roberto Miccoli, Sebastiano Calandra and Stefano Bertolini
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Association of HLA Typing with Nicotine Dependence by Extraction of Salivary DNA among Indian Population
Research Article: J Genet Disor Genet Rep, 7:1
DOI: 10.4172/2327-5790.1000170
Purohit A, Purohit BM, Mani A and Bhambal A
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Patterns of Utilization of Genetic Services Following the Initiation of Community based Primary Care Carrier Screening in a Traditional Muslim Community
Research Article: J Genet Disor Genet Rep, 7:2
DOI: 10.4172/2327-5790.1000175
Abu-Rabia R, Abo Rabia A, Birk O and Elana Shoham-Vardi
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Spectrum of CFTR Mutations in the Algerian Population: Molecular and Computational Analysis
Research Article: J Genet Disor Genet Rep 2016, 5:1
DOI: 10.4172/2327-5790.1000130
Fatima Zohra Sediki, Abdelkarim Radoui, Abdallah Boudjema, Meriem Abdi, Faouzia Zemani-Fodil, Nadhira Saidi-Mehtar and Faiza Cabet
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The Prevalence of Three Common MEFV Gene Mutations in West Bank Population among Students of Najah National University, Palestine
Research Article: J Genet Disor Genet Rep, 6:4
DOI: 10.4172/2327-5790.1000166
Tanbour RG, Sawafta TS and Basha WS
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Phenylketonuria (PKU) - What Next? Mini-Review
Review Article: J Genet Disor Genet Rep 2013, 2:2
DOI: 10.4172/2327-5790.1000108
WB Hanley
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Cerebrovascular and Brain Abnormalities in Autosomal- Dominant Polycystic Kidney Disease: Role of 3d Time-of-Flight Magnetic Resonance Angiography
Research Article: J Genet Disor Genet Rep 2016, 5:3
DOI: 10.4172/2327-5790.1000140
Carmela Russo, Ferdinando Caranci, Massimo Imbriaco, Manuela Napoli, Antonio Pisani, Eleonora Riccio, Michele Santangelo, Sirio Cocozza, Enrico Tedeschi, Francesco Briganti and Arturo Brunetti
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Atypical Hypotonia-Cystinuria a New Case: Genotype-Phenotype, Description
Case Report: J Genet Disor Genet Rep, 7:3
DOI: 10.4172/2327-5790.1000180
Preka Evgenia, Ariane Paoloni-Giacobino, Frédérique Sloan-Béna, Paloma Parvex and Alexandra Wilhelm-Bals
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Pirimiphos-methyl Resistance in Culex pipiens (Diptera: Culicidae) in Southern Tunisia
Research Article: J Genet Disor Genet Rep, 6:2
DOI: 10.4172/2327-5790.1000155
Tabbabi Ahmed, Daaboub Jaber, Laamari Ali, Ben Cheikh Raja and Ben Cheikh Hassen
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Variation of Abnormal Hemoglobins Concentrated in Durg, Chhattisgarh: A Brief Note Based on Cross-Sectional Study
Case Report: J Genet Disor Genet Rep 2016, 5:2
DOI: 10.4172/2327-5790.1000135
Devendra Lingojwar, Pramod Gupta, Savita Bhutoria, Sarita Lingojwar, Nikhil Mishra, Anil Kumar
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Chlorpyrifos Resistance Characteristics of Culex pipiens (Diptera: Culicidae) from Northern Tunisia
Research Article: J Genet Disor Genet Rep, 6:3
DOI: 10.4172/2327-5790.1000161
Jaber Daaboub, Ahmed Tabbabi, Ali Lamari, Mohamed Feriani, Chokri Boubaker and Hassen Ben Cheikh
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Erring on the Side of Life: Children with Rare Trisomy Conditions, Medical Interventions and Quality of Life
Review Article: J Genet Disor Genet Rep 2013, 2:1
DOI: 10.4172/2327-5790.1000103
Deborah A. Bruns
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Involvement of TLR4 Polymorphisms on Colorectal Cancer Treatment
Research Article: J Genet Disor Genet Rep, 7:1
DOI: 10.4172/2327-5790.1000171
Omrane I, Baroudi O, Medimegh I, Ayari H, Kourda N, Mezlini A, Bougatef K and Benammar-Elgaaied A
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Advances of Programmed Death-1/Programmed Death-1 Ligand Signal Pathway and its Blockers in Nasopharyngeal Carcinoma
Review Article: J Genet Disor Genet Rep, 7:2
DOI: 10.4172/2327-5790.1000176
Zhou Q, Assani G, Ling H, Xiong Y and Zhou Y
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Telomeres in Cancer: Length, Positioning and Epigenetics
Review Article: J Genet Disor Genet Rep 2016, 5:1
DOI: 10.4172/2327-5790.1000131
Patel TN, Sulekha R Nair, Lekshmi Mohan, Fahmina Y, Ashwini, Devi S and VA Saimadhukiran Dabbiru
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Expression of TCTP-Related Genes
Research Article: J Genet Disor Genet Rep, 6:2
DOI: 10.4172/2327-5790.1000156
Jun-ichi Kashiwakura and Toshiaki Kawakami
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Genotype and Allele Frequencies of Calcium-Sensing Receptor Gene a986s (rs1801725) Polymorphism in Saudi Adults
Research Article: J Genet Disor Genet Rep 2016, 5:3
DOI: 10.4172/2327-5790.1000141
Sonbol HS and Al Otaibi WF
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Genotype-phenotype characteristics of β thalassemia children in the Gaza Strip, Palestine
Research Article: J Genet Disor Genet Rep 2013, 2:2
DOI: 10.4172/2327-5790.1000109
Maged M Yassin, Mahmoud M Sirdah, Rami M Al Haddad, Abdel-Monem H. Lubbad and Mansour S Al-Yazji
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Cleidocranial Dysplasia in a Mother and her New-born Daughter
Case Report: J Genet Disor Genet Rep 2016, 5:2
DOI: 10.4172/2327-5790.1000136
Ma?gorzata Napieralska, Aleksandra Modlinska, Tomasz Rybkiewicz, Regina ?uralska
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Parental Consanguinity and Birth Defects in Lebanon: The National Collaborative Perinatal Neonatal Network (NCPNN)
Research Article: J Genet Disor Genet Rep, 7:3
DOI: 10.4172/2327-5790.1000181
Farra C, El Rafei R, Mumtaz G, Charafeddine L, Tlays F and Yunis K
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Morbid Obesity and Psychiatric Disorders Hiding a Sex Aneuploidy: A Case of Late Diagnosis of 48,XXYY Syndrome
Case Report: J Genet Disor Genet Rep, 6:3
DOI: 10.4172/2327-5790.1000162
Antía Fernández-Pombo, Pablo San Millán-Tejedor, Cristina Guillín-Amarelle, Ana I. Castro, Juan Carlos Guinarte-Cabada, Margarita Ventura-Victoria and David Araújo-Vilar
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Evaluation of Fenitrothion against Culex pipiens (Diptera: Culicidae) Larvae in Grand Tunis Area of Tunisia
Research Article: J Genet Disor Genet Rep, 6:2
DOI: 10.4172/2327-5790.1000157
Ahmed Tabbabi, Jaber Daaboub, Ali Lamari, Raja Ben Cheikh, Ibtissem Ben Jha and Hassen Ben Cheikh
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Mini Review: HLA B27 and its Immunogenetics in Ankylosing Spondylitis
Review Article: J Genet Disor Genet Rep 2013, 2:1
DOI: 10.4172/2327-5790.1000104
Hamid Nawaz Tipu