Sandra M. Cooke

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Active since

2008

Affiliations

National Institute on Deafness and Other Communication Disorders(Current)

Sandra M. Cooke is an author at National Institute on Deafness and Other Communication Disorders specializing in genetics, human genetics, and life sciences.

Publications per year

2008–2011

Publications

Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15

Lance P. Doucette, Nancy D. Merner, Sandra M. Cooke et al. · European Journal of Human Genetics · 2008 · 39 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

A novel deletion partly removing the <i>AVP</i> gene causes autosomal recessive inheritance of early‐onset neurohypophyseal diabetes insipidus

Helene Kvistgaard, Jane Hagelskjær Knudsen, Guftar Shaikh et al. · Clinical Genetics · 2011 · 24 citations

Life Sciences, Endocrinology, Genetics +16

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