Unknown diagnosis in two male cousins with facial abnormalities, optic atrophy, abnormal EEG, and severe psychomotor retardation-Reference-Cited by-同舟云学术

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Unknown diagnosis in two male cousins with facial abnormalities, optic atrophy, abnormal EEG, and severe psychomotor retardation

Published:2002-12-11 Issue:4 Volume:116A Page:381-384
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Mégarbané André

Funder

The Saint Joseph University in Beirut, Lebanon

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference7 articles.

1. POSSUM: Pictures of standard syndromes and undiagnosed malformations;Bankier;Murdoch Childrens Research Institute,2001

2. Teratogenic viral infections;Dickinson;Clin Obstet Gynecol,1990

3. The carbohydrate-deficient glycoprotein syndromes: An overview;Jaeken;J Inherit Metab Dis,1993

4. Predicting the outcome of symptomatic congenital cytomegalovirus infection;Jones;J Paediatr Child Health,1995

5. A syndrome of severe mental retardation, spasticity, and tapetoretinal degeneration linked to chromosome 15q24;Mitchell;Am J Hum Genet,1998

Cited by 2 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. New Syndromes First Reported Among Arabs;Genetic Disorders Among Arab Populations;2010

2. Optic Atrophy in Children;Pediatric Neuro-Ophthalmology;2009-12-09

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