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Xiaoyan Cindy Li

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Otolaryngologic Clinics of North America|October 24, 2002
Nonsyndromic hereditary hearing lossXiaoyan Cindy Li, Rick A Friedman
BMC Medical Genetics|September 28, 2004
Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and PakistanZubair M Ahmed, Xiaoyan Cindy Li, Shontell D Powell, et al.
European Journal of Human Genetics : EJHG|December 25, 2008
Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15Lance Doucette, Nancy D Merner, Sandra Cooke, et al.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Otolaryngologic Clinics of North America|October 24, 2002
Nonsyndromic hereditary hearing lossXiaoyan Cindy Li, Rick A Friedman
BMC Medical Genetics|September 28, 2004
Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and PakistanZubair M Ahmed, Xiaoyan Cindy Li, Shontell D Powell, et al.
European Journal of Human Genetics : EJHG|December 25, 2008
Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15Lance Doucette, Nancy D Merner, Sandra Cooke, et al.
Pageof 1