Cytogenetic Diagnosis of Fragile X Syndrome: Study of 305 Suspected Cases in Saudi Arabia-Reference-Cited by-同舟云学术

Cytogenetic Diagnosis of Fragile X Syndrome: Study of 305 Suspected Cases in Saudi Arabia

Published:2000-05 Issue:3-4 Volume:20 Page:214-217
ISSN:0256-4947
Container-title:Annals of Saudi Medicine
language:en
Short-container-title:Ann Saudi Med

Author:

Iqbal M. Anwar¹,Sakati Nadia¹,Nester Michael¹,Ozand Pinar¹

Affiliation:

1. From the Departments of Pathology, Section of Cytogenetics/Molecular Genetics, Pediatrics, Sections of Pediatric Genetics/Endocrinology and Metabolic Diseases, and Neurosciences, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia

Publisher

King Faisal Specialist Hospital and Research Centre

Subject

General Medicine

Reference41 articles.

1. The marker (X) syndrome: a cytogenetic and genetic analysis;Sherman SL;Ann Hum Genet,1984

2. Further segregation analysis of the fragile X syndrome with special reference to transmitting males;Sherman SL;Hum Genet,1985

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