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American Journal of Human Genetics|December 15, 2000

DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24C C Greene, P M McMillan, S E Barker, et al.

Virology|January 9, 2001

The sequence and antiapoptotic functional domains of the human cytomegalovirus UL37 exon 1 immediate early protein are conserved in multiple primary strainsW A Hayajneh, A M Colberg-Poley, A Skaletskaya, et al.

Human Molecular Genetics|October 1, 1995

A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3M M Lesperance, J W Hall, F H Bess, et al.

Journal of Medical Genetics|July 29, 1999

A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locusG Van Camp, H Kunst, K Flothmann, et al.

Human Molecular Genetics|November 16, 2001

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing lossI N Bespalova, G Van Camp, S J Bom, et al.

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Showing results (11-20 of 15) with videos related to

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You have reached the last page of results.This site can display upto 15 results.

American Journal of Human Genetics|December 15, 2000

DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24C C Greene, P M McMillan, S E Barker, et al.

Virology|January 9, 2001

The sequence and antiapoptotic functional domains of the human cytomegalovirus UL37 exon 1 immediate early protein are conserved in multiple primary strainsW A Hayajneh, A M Colberg-Poley, A Skaletskaya, et al.

Human Molecular Genetics|October 1, 1995

A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3M M Lesperance, J W Hall, F H Bess, et al.

Journal of Medical Genetics|July 29, 1999

A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locusG Van Camp, H Kunst, K Flothmann, et al.

Human Molecular Genetics|November 16, 2001

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing lossI N Bespalova, G Van Camp, S J Bom, et al.

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