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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Main Authors: Molinari Laura M (Author), Bacino Carlos A (Author), Phillips Michael (Author), Fernbach Susan D (Author), Safiullah Arsalan M (Author), Lalani Seema R (Author), Glass Nancy L (Author), Towbin Jeffrey A (Author), Craigen William J (Author), Belmont John W (Author)
Format: Book
Published: BMC, 2005-02-01T00:00:00Z.
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