Biography
Dr. Barry J Byrne is currently Director of UF Powell Gene Therapy Center at the same time Professor of Pediatrics and Molecular Genetics & Microbiology and Associate Chair of Pediatrics at University of Florida. Dr. Barry J Byrne's laboratory is focused on understanding the pathophysiology of inherited cardioskeletal myopathies and therapeutic strategies using gene therapy. Specifically, they have developed novel gene therapies for neuromuscular diseases such as Pompe disease. The disease is characteristic of many muscle diseases which lead to skeletal and cardiac muscle weakness. Dr. Barry J Byrne has used AAV vectors to achieve sustained correction of the gene deficiency in Pompe disease models leading to restoration of contractile and metabolic function of striated muscle and motor nerves. Recently, Dr. Barry J Byrne has incorporated novel combinations of AAV serotypes and/or capsid modifications with tissue-specific promoters to direct gene transduction and expression of the therapeutic transgene. Dr. Barry J Byrne approach (AAV) is now being evaluated in a human clinical trial investigating the safety and efficacy of direct gene delivery to the diaphragm.
Research Interest
Dr. Barry J Byrne's research interests includes:
Adeno-associated virus mediated gene transfer in the cardiovascular system and striated muscle, Cell therapy in cardiovascular disease, Gene therapy for muscular dystrophy (Pompe disease and DMD), Mechanisms of allograft tolerance in cardiac transplantation and Cardiac development.
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Genotype is Alluded to as Heterozygous
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Roger Federer*
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Basin Mahar
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Root Willson*
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Woakes Chris*
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Williamson Kristen*
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Effect and Co-operations among Smoking and Customary Prognostic Elements
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Jordan Kate*
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Young Scientist Awards at Genome Editing 2020 for the best researches in Genome Editing and Gene Therapy
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William J. Rowe
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Rajinder Kaul
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Bioinformatics
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Genetic Brain Disorders
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DNA: Desoxyribonucleic Acid
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Genetic Epidemiology
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Young Researchers Forum: Young Scientist Awards for Genetics 2020
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Gail Risbridge
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Young Researchers Forum: Young Scientist Awards for System Biology 2020
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Gottfried Baier
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Maternal and Paternal Age at Pregnancy for Low Incidence Trisomy Groups: Preliminary Findings and Implications
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Cross-Sectional Cohort Ukrainian Megapolice Sample Study of People�s Reactions to Faces of Patients with Different Mental Conditions
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Biotinidase Deficiency Presenting as Hyperventilation Syndrome
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Farid Ahmed
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X-Linked Inheritance and Dominance: Clinical Insights and Management Strategies
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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