December | 2016 | Journal of Genetic Disorders Genetic Reports

Journal of Genetic Disorders & Genetic ReportsISSN: 2327-5790

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Volume 5, Issue 4

Article(s) in December Issue

Research Article

J Genet Disor Genet Rep, 5:4

10.4172/2327-5790.1000142

Chromosome 22q11.2 and 7q11.23 Microdeletions in Children with Congenital Heart Defects Detected by Fish Technique

Mirea AM, Popp RA, Lazea C, Cuzmici Z, Al Khzouz C, Bucerzan S, Nascu, Man S, Iurian S, Miclea DL

Case Report

J Genet Disor Genet Rep, 5:4

10.4172/2327-5790.1000143

Treatment with Agalsidase Alfa during Pregnancy in a Heterozygous Female with Fabry Disease

Antonio Pisani, Giuseppe Bifulco, Attilio Di Spiezio Sardo and Eleonora Riccio

Research Article

J Genet Disor Genet Rep, 5:4

10.4172/2327-5790.1000144

Screening of Genetic Mutations in GBA1, GIGYF2 and VPS35 in Parkinson Disease Patients from India

Tamali Halder, Janak Raj, Sharad Pandey, Ajay Kumar, Sagar Kawale, Sandeep Chaudhary, Vivek Sharma, Deepika Joshi and Parimal Das

Case Report

J Genet Disor Genet Rep, 5:4

10.4172/2327-5790.1000145

Smith-Magenis Syndrome Treated with Ramelteon and Amphetamine-dextroamphetamine: Case Report and Review of the Literature

Baek WS, Elsea SH

Research Article

J Genet Disor Genet Rep, 5:4

10.4172/2327-5790.1000146

Same Mutation in Two Patients with Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome) Coming from Different Municipalities in the Department of Cauca, Southwestern Colombia

Acosta MA, Lago RM, Barros F and Carracedo AM

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Citations : 160

Journal of Genetic Disorders & Genetic Reports received 160 citations as per Google Scholar report

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Volume 5, Issue 4

Chromosome 22q11.2 and 7q11.23 Microdeletions in Children with Congenital Heart Defects Detected by Fish Technique

Treatment with Agalsidase Alfa during Pregnancy in a Heterozygous Female with Fabry Disease

Screening of Genetic Mutations in GBA1, GIGYF2 and VPS35 in Parkinson Disease Patients from India

Smith-Magenis Syndrome Treated with Ramelteon and Amphetamine-dextroamphetamine: Case Report and Review of the Literature

Same Mutation in Two Patients with Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome) Coming from Different Municipalities in the Department of Cauca, Southwestern Colombia

Track Your Manuscript

Explore SciTechnol

Google Scholar citation report

Citations : 160

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