Screening of subtle copy number changes in Aicardi syndrome patients with a high resolution X chromosome array-CGH-Reference-Cited by-同舟云学术

Screening of subtle copy number changes in Aicardi syndrome patients with a high resolution X chromosome array-CGH

Published:2007-09 Issue:5 Volume:50 Page:386-391
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Yilmaz Saliha,Fontaine Hervé,Brochet Karène,Grégoire Marie-José,Devignes Marie-Dominique,Schaff Jean-Luc,Philippe Christophe,Nemos Christophe,McGregor John Louis,Jonveaux Philippe

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference12 articles.

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3. Facial and physical features of Aicardi syndrome: infants to teenagers;Sutton;Am. J. Med. Genet.,2005

4. Aicardi syndrome in two sisters;Molina;J. Pediatr.,1989

5. The Aicardi syndrome in a 47, XXY male;Hopkins;Aust. Paediatr. J.,1979

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1. Aicardi Syndrome Is a Genetically Heterogeneous Disorder;Genes;2023-07-31

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3. Aicardi syndrome, an unsolved mystery: Review of diagnostic features, previous attempts, and future opportunities for genetic examination;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2018-12-10

4. Independent variant analysis ofTEAD1andOCEL1in 38 Aicardi syndrome patients;Molecular Genetics & Genomic Medicine;2017-01-25

5. Exome Sequencing Fails to Identify the Genetic Cause of Aicardi Syndrome;Molecular Syndromology;2016