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Molecular and Cellular Probes
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June 20, 1998
A PAX3 polymorphism (T315K) in a family exhibiting Waardenburg Syndrome type 2
C 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 DFNB9
S 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 families
A 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 dysfunction
S 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 Xp21.2
A 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 1F
Z 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 gene
P 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 degeneration
A 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 DFNB3
A 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 6
M E O'Neill, J Marietta, D Nishimura, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 28) with videos related to
Sort By:
Page
of 3
Molecular and Cellular Probes
|
June 20, 1998
A PAX3 polymorphism (T315K) in a family exhibiting Waardenburg Syndrome type 2
C 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 DFNB9
S 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 families
A 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 dysfunction
S 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 Xp21.2
A 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 1F
Z 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 gene
P 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 degeneration
A 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 DFNB3
A 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 6
M E O'Neill, J Marietta, D Nishimura, et al.
Page
of 3