Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss

Published 2010 View Full Article

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Title
Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss
Authors
Keywords
-
Journal
Journal of Genetics and Genomics
Volume 37, Issue 12, Pages 787-793
Publisher
Elsevier BV
Online
2010-12-29
DOI
10.1016/s1673-8527(09)60096-5

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