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The Journal of Biological Chemistry
|
April 5, 1993
Binding of Ku protein to DNA. Measurement of affinity for ends and demonstration of binding to nicks
P R Blier, A J Griffith, J Craft, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
July 11, 2000
Audiovestibular phenotype associated with a COL11A1 mutation in Marshall syndrome
A J Griffith, S S Gebarski, N T Shepard, et al.
Molecular Biology Reports
|
May 1, 1992
Nucleotide sequence and genomic structure analyses of the p70 subunit of the human Ku autoantigen: evidence for a family of genes encoding Ku (p70)-related polypeptides
A J Griffith, J Craft, J Evans, et al.
Human Genetics
|
May 26, 1998
Gene symbol: COL11A1. Disease: Marshall syndrome
M H Meisler, A J Griffith, M Warman, et al.
Journal of Craniofacial Genetics and Developmental Biology
|
December 10, 1999
Optic, olfactory, and vestibular dysmorphogenesis in the homozygous mouse insertional mutant Tg9257
A J Griffith, W Ji, M E Prince, et al.
Advances in Oto-Rhino-Laryngology
|
November 1, 2002
Hearing impairment in Stickler syndrome
R J C Admiraal, Y M Szymko, A J Griffith, et al.
The Laryngoscope
|
August 1, 1996
Familial large vestibular aqueduct syndrome
A J Griffith, A Arts, C Downs, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1990
Isolation and characterization of cDNA encoding the 80-kDa subunit protein of the human autoantigen Ku (p70/p80) recognized by autoantibodies from patients with scleroderma-polymyositis overlap syndrome
T Mimori, Y Ohosone, N Hama, et al.
The Laryngoscope
|
September 17, 1998
Familial Mondini dysplasia
A J Griffith, S A Telian, C Downs, et al.
Journal of Medical Genetics
|
April 3, 2004
Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6)
S A Mohiddin, Z M Ahmed, A J Griffith, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 41) with videos related to
Sort By:
Page
of 5
The Journal of Biological Chemistry
|
April 5, 1993
Binding of Ku protein to DNA. Measurement of affinity for ends and demonstration of binding to nicks
P R Blier, A J Griffith, J Craft, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
July 11, 2000
Audiovestibular phenotype associated with a COL11A1 mutation in Marshall syndrome
A J Griffith, S S Gebarski, N T Shepard, et al.
Molecular Biology Reports
|
May 1, 1992
Nucleotide sequence and genomic structure analyses of the p70 subunit of the human Ku autoantigen: evidence for a family of genes encoding Ku (p70)-related polypeptides
A J Griffith, J Craft, J Evans, et al.
Human Genetics
|
May 26, 1998
Gene symbol: COL11A1. Disease: Marshall syndrome
M H Meisler, A J Griffith, M Warman, et al.
Journal of Craniofacial Genetics and Developmental Biology
|
December 10, 1999
Optic, olfactory, and vestibular dysmorphogenesis in the homozygous mouse insertional mutant Tg9257
A J Griffith, W Ji, M E Prince, et al.
Advances in Oto-Rhino-Laryngology
|
November 1, 2002
Hearing impairment in Stickler syndrome
R J C Admiraal, Y M Szymko, A J Griffith, et al.
The Laryngoscope
|
August 1, 1996
Familial large vestibular aqueduct syndrome
A J Griffith, A Arts, C Downs, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1990
Isolation and characterization of cDNA encoding the 80-kDa subunit protein of the human autoantigen Ku (p70/p80) recognized by autoantibodies from patients with scleroderma-polymyositis overlap syndrome
T Mimori, Y Ohosone, N Hama, et al.
The Laryngoscope
|
September 17, 1998
Familial Mondini dysplasia
A J Griffith, S A Telian, C Downs, et al.
Journal of Medical Genetics
|
April 3, 2004
Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6)
S A Mohiddin, Z M Ahmed, A J Griffith, et al.
Page
of 5