Syndromic Congenital Sensorineural Deafness, Microtia and Microdontia Resulting From a Novel Homoallelic Mutation in Fibroblast Growth Factor 3 (FGF3)
European Journal of Human Genetics - United Kingdom
doi 10.1038/ejhg.2008.141
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August 13, 2008
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Springer Science and Business Media LLC