Frequency ofFMR1gene mutation and CGG repeat polymorphism in intellectually disabled children in Pakistan-Reference-Cited by-同舟云学术

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Frequency ofFMR1gene mutation and CGG repeat polymorphism in intellectually disabled children in Pakistan

Published:2014-01-29 Issue:5 Volume:164 Page:1151-1161
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet

Author:

Fatima Tasneem¹,Zaidi Syed Aley Hasan²,Sarfraz Noorjehan¹,Perween Siddiqa¹,Khurshid Faraz¹,Imtiaz Fauzia³

Affiliation:

1. Department of Biological and Biomedical Sciences; Aga Khan University; Karachi Pakistan

2. Department of Pathology; Hamdard College of Medicine and Dentistry Hamdard University; Karachi Pakistan

3. Department of Biochemistry; Dow International University; Karachi Pakistan

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference59 articles.

1. Primary health care: What is it and what is it not? Views of teaching faculty at an undergraduate medical college in Pakistan;Abbas;East Mediterr Health J,2012

2. Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family;Ahmad;Am J Med Genet,2001

3. The population of persons with disabilities in Pakistan;Ahmed;Asia Pac Popul J,1995

4. Analysis of fragile X trinucleotide repeat in Basques: Association of premutation and intermediate sizes, anchoring AGGs and linked microsatellites with unstable alleles;Arrieta;Curr Genomics,2008

5. Triplet repeat polymorphism & fragile X syndrome in the Indian context;Baskaran;Indian J Med Res,1998

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. FMR1 Gene Mutation Analysis and CGG Repeat Number Distribution from a Single Center;Gazi Medical Journal;2022-10-01

2. Sex chromosomes-linked single-gene disorders involved in human infertility;European Journal of Medical Genetics;2019-09

3. Advances in identification of genes involved in autosomal recessive intellectual disability: a brief review;Journal of Medical Genetics;2019-03-06

4. Prevalence of Fragile X Syndrome among children receiving special education and carrier states in first degree relatives.;Ceylon Medical Journal;2017-06-30

5. Epidemiology of Fragile X Syndrome;Fragile X Syndrome;2017

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