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The Yale Journal of Biology and Medicine
|
January 1, 1992
Biological and clinical aspects of autoimmune inner ear disease
A J Griffith
Journal of Medical Genetics
|
July 4, 2001
Genetic analysis of the connexin-26 M34T variant
A J Griffith
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
January 1, 1996
Transsphenoid endoscopic management of petrous apex cholesterol granuloma
A J Griffith, J E Terrell
Nature Genetics
|
April 7, 1999
Making sense out of sound
A J Griffith, T B Friedman
Gene
|
May 15, 1992
The murine gene encoding the highly conserved Sm B protein contains a nonfunctional alternative 3' splice site
A J Griffith, C Schmauss, J Craft
Neuroscience
|
September 13, 2015
Progressive irreversible hearing loss is caused by stria vascularis degeneration in an Slc26a4-insufficient mouse model of large vestibular aqueduct syndrome
T Ito, A Nishio, P Wangemann, et al.
Oral Diseases
|
June 5, 2016
Unresolved questions regarding human hereditary deafness
A U Rehman, T B Friedman, A J Griffith
Clinical Genetics
|
January 26, 2007
A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1
S Kitajiri, T Makishima, T B Friedman, et al.
Journal of Medical Genetics
|
March 18, 2009
Do mutations of the Pendred syndrome gene, SLC26A4, confer resistance to asthma and hypertension?
A C Madeo, A Manichaikul, S P Pryor, et al.
The Journal of Biological Chemistry
|
January 5, 1992
Ku polypeptides synthesized in vitro assemble into complexes which recognize ends of double-stranded DNA
A J Griffith, P R Blier, T Mimori, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 41) with videos related to
Sort By:
Page
of 5
The Yale Journal of Biology and Medicine
|
January 1, 1992
Biological and clinical aspects of autoimmune inner ear disease
A J Griffith
Journal of Medical Genetics
|
July 4, 2001
Genetic analysis of the connexin-26 M34T variant
A J Griffith
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
January 1, 1996
Transsphenoid endoscopic management of petrous apex cholesterol granuloma
A J Griffith, J E Terrell
Nature Genetics
|
April 7, 1999
Making sense out of sound
A J Griffith, T B Friedman
Gene
|
May 15, 1992
The murine gene encoding the highly conserved Sm B protein contains a nonfunctional alternative 3' splice site
A J Griffith, C Schmauss, J Craft
Neuroscience
|
September 13, 2015
Progressive irreversible hearing loss is caused by stria vascularis degeneration in an Slc26a4-insufficient mouse model of large vestibular aqueduct syndrome
T Ito, A Nishio, P Wangemann, et al.
Oral Diseases
|
June 5, 2016
Unresolved questions regarding human hereditary deafness
A U Rehman, T B Friedman, A J Griffith
Clinical Genetics
|
January 26, 2007
A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1
S Kitajiri, T Makishima, T B Friedman, et al.
Journal of Medical Genetics
|
March 18, 2009
Do mutations of the Pendred syndrome gene, SLC26A4, confer resistance to asthma and hypertension?
A C Madeo, A Manichaikul, S P Pryor, et al.
The Journal of Biological Chemistry
|
January 5, 1992
Ku polypeptides synthesized in vitro assemble into complexes which recognize ends of double-stranded DNA
A J Griffith, P R Blier, T Mimori, et al.
Page
of 5