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T B Friedman

Showing results (61-70 of 86) with videos related to

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Clinical Genetics|August 5, 2009
DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15A M Waryah, A Rehman, Z M Ahmed, et al.
Journal of Medical Genetics|August 3, 2004
Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunctionS Naz, A J Griffith, S Riazuddin, et al.
The American Journal of Pathology|October 5, 2001
Myosin XVA expression in the pituitary and in other neuroendocrine tissues and tumorsR V Lloyd, S Vidal, L Jin, et al.
Clinical Genetics|February 19, 2008
A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1L M Peters, R A Fridell, E T Boger, et al.
American Journal of Human Genetics|June 9, 2001
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1FZ M Ahmed, S Riazuddin, S L Bernstein, et al.
American Journal of Human Genetics|May 11, 1992
Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortiumL A Farrer, K M Grundfast, J Amos, et al.
Clinical Genetics|September 20, 2007
Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in PakistanS-I Kitajiri, R McNamara, T Makishima, et al.
American Journal of Medical Genetics|August 22, 1997
Exclusion of BMP6 as a candidate gene for cleidocranial dysplasiaJ W Innis, J H Asher, Y Liang, et al.
American Journal of Human Genetics|October 1, 1994
Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypesL A Farrer, K S Arnos, J H Asher, et al.
Human Molecular Genetics|August 1, 2000
The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cellsD W Anderson, F J Probst, I A Belyantseva, et al.
Pageof 9

Showing results (61-70 of 86) with videos related to

Sort By:
Pageof 9
Clinical Genetics|August 5, 2009
DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15A M Waryah, A Rehman, Z M Ahmed, et al.
Journal of Medical Genetics|August 3, 2004
Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunctionS Naz, A J Griffith, S Riazuddin, et al.
The American Journal of Pathology|October 5, 2001
Myosin XVA expression in the pituitary and in other neuroendocrine tissues and tumorsR V Lloyd, S Vidal, L Jin, et al.
Clinical Genetics|February 19, 2008
A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1L M Peters, R A Fridell, E T Boger, et al.
American Journal of Human Genetics|June 9, 2001
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1FZ M Ahmed, S Riazuddin, S L Bernstein, et al.
American Journal of Human Genetics|May 11, 1992
Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortiumL A Farrer, K M Grundfast, J Amos, et al.
Clinical Genetics|September 20, 2007
Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in PakistanS-I Kitajiri, R McNamara, T Makishima, et al.
American Journal of Medical Genetics|August 22, 1997
Exclusion of BMP6 as a candidate gene for cleidocranial dysplasiaJ W Innis, J H Asher, Y Liang, et al.
American Journal of Human Genetics|October 1, 1994
Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypesL A Farrer, K S Arnos, J H Asher, et al.
Human Molecular Genetics|August 1, 2000
The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cellsD W Anderson, F J Probst, I A Belyantseva, et al.
Pageof 9