SNP genotyping to screen for a common deletion in CHARGE Syndrome

SNP genotyping to screen for a common deletion in CHARGE Syndrome

<p>Abstract</p> <p>Background</p> <p>CHARGE syndrome is a complex of birth defects including coloboma, choanal atresia, ear malformations and deafness, cardiac defects, and growth delay. We have previously hypothesized that CHARGE syndrome could be caused by unidentifie...

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Bibliographic Details
Main Authors: Molinari Laura M, Bacino Carlos A, Phillips Michael, Fernbach Susan D, Safiullah Arsalan M, Lalani Seema R, Glass Nancy L, Towbin Jeffrey A, Craigen William J, Belmont John W
Format: Article
Language:English
Published: BMC 2005-02-01
Series:BMC Medical Genetics
Online Access:http://www.biomedcentral.com/1471-2350/6/8

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http://www.biomedcentral.com/1471-2350/6/8

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