W. J. Kimberling

OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele

Renée Varga, Matthew R. Avenarius, Philip M. Kelley et al. · Journal of Medical Genetics · 2005 · 169 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Duplication-deficiency of the short arm of chromosome 8 following artificial insemination.

Richard G. Weleber, Ram S. Verma, W. J. Kimberling et al. · PubMed · 1976 · 82 citations

Life Sciences, Genetics, Molecular Genetics +12

Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese

Jiro Akita, Satoko Abe, Hideichi Shinkawa et al. · Journal of Human Genetics · 2001 · 42 citations

Life Sciences, Genetics, Molecular Genetics +12

Variable hearing impairment in a DFNB2 family with a novel <i>MYO7A</i> missense mutation

Michael S. Hildebrand, N. Thorne, C.J. Bromhead et al. · Clinical Genetics · 2010 · 40 citations

Life Sciences, Genetics, Molecular Genetics +17

Localization of spherocytosis to chromosome 8 or 12 and report of a family with spherocytosis and a reciprocal translocation.

W. J. Kimberling, T. Fulbeck, Linda Dixon et al. · PubMed · 1975 · 39 citations

Life Sciences, Genetics, Molecular Genetics +6