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E R Wilcox

Showing results (11-20 of 28) with videos related to

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Molecular and Cellular Probes|June 20, 1998
A PAX3 polymorphism (T315K) in a family exhibiting Waardenburg Syndrome type 2C Wang, E Kim, A Attaie, et al.
American Journal of Human Genetics|July 21, 2000
OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9S Yasunaga, M Grati, S Chardenoux, et al.
American Journal of Human Genetics|January 1, 1995
Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type 1 in two familiesA K Lalwani, J R Brister, J Fex, 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.
American Journal of Human Genetics|October 1, 1994
A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2A K Lalwani, J R Brister, J Fex, 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.
Genomics|July 8, 1998
A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C geneP K Jain, A K Lalwani, X C Li, et al.
Audiology & Neuro-Otology|May 1, 1997
A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degenerationA K Lalwani, F H Linthicum, E R Wilcox, et al.
Science (New York, N.Y.)|June 20, 1998
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3A Wang, Y Liang, R A Fridell, et al.
Human Molecular Genetics|June 1, 1996
A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6M E O'Neill, J Marietta, D Nishimura, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Molecular and Cellular Probes|June 20, 1998
A PAX3 polymorphism (T315K) in a family exhibiting Waardenburg Syndrome type 2C Wang, E Kim, A Attaie, et al.
American Journal of Human Genetics|July 21, 2000
OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9S Yasunaga, M Grati, S Chardenoux, et al.
American Journal of Human Genetics|January 1, 1995
Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type 1 in two familiesA K Lalwani, J R Brister, J Fex, 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.
American Journal of Human Genetics|October 1, 1994
A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2A K Lalwani, J R Brister, J Fex, 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.
Genomics|July 8, 1998
A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C geneP K Jain, A K Lalwani, X C Li, et al.
Audiology & Neuro-Otology|May 1, 1997
A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degenerationA K Lalwani, F H Linthicum, E R Wilcox, et al.
Science (New York, N.Y.)|June 20, 1998
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3A Wang, Y Liang, R A Fridell, et al.
Human Molecular Genetics|June 1, 1996
A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6M E O'Neill, J Marietta, D Nishimura, et al.
Pageof 3