A chromosomal microdeletion of 15q in a female patient with epilepsy, ID, and autism spectrum disorder: a case report-Reference-Cited by-同舟云学术

A chromosomal microdeletion of 15q in a female patient with epilepsy, ID, and autism spectrum disorder: a case report

Published:2017-05-12 Issue:6 Volume:5 Page:1013-1017
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Ahram Dina F.¹^ORCID,Al-Sarraj Yasser²,Taha Rowaida Z.²,Elhag Saba F.²,Al-Shaban Fouad A.²,El-Shanti Hatem³⁴,Kambouris Marios⁵⁶

Affiliation:

1. Division of Nephrology; College of Physicians and Surgeons; Columbia University; New York City New York

2. Medical Genetics Center; Qatar Biomedical Research Institute; Hamad Bin Khalifa University; Doha Qatar

3. Pediatrics; University of Jordan; Amman Jordan

4. Pediatrics; University of Iowa; Iowa City Iowa

5. Pathology-Genetics; Sidra Medical and Research Center; Doha Qatar

6. Genetics; Yale University School of Medicine; New Haven Connecticut

Funder

Qatar National Research Fund

Publisher

Wiley

Subject

General Medicine

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3. Autism as a strongly genetic disorder: evidence from a British twin study;Bailey;Psychol. Med.,1995

4. Prevalence of autism spectrum disorders-Autism and Developmental Disabilities Monitoring Network, 14 sites, United States, 2008;Autism, Developmental Disabilities Monitoring Network Surveillance Year Principal Investigators, Centers for Disease Control and Prevention;MMWR Surveill. Summ.,2012

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