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American Journal of Human Genetics
|
August 26, 2000
A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration
A Rivera, K White, H Stöhr, et al.
Gynecologic Oncology
|
March 4, 1999
Frequency of BRCA1 mutation 5382insC in German breast cancer patients
J Backe, S Hofferbert, B Skawran, et al.
The British Journal of Ophthalmology
|
July 24, 2001
Evaluation of the G protein coupled receptor-75 (GPR75) in age related macular degeneration
C G Sauer, K White, H Stöhr, et al.
American Journal of Human Genetics
|
June 23, 1998
Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q
R E Kelsell, K Gregory-Evans, C Y Gregory-Evans, et al.
Genomics
|
April 15, 1997
A sequence-ready high-resolution physical map of the best macular dystrophy gene region in 11q12-q13
P R Cooper, N J Nowak, M J Higgins, et al.
Nature Genetics
|
July 14, 1998
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
T M Strom, G Nyakatura, E Apfelstedt-Sylla, et al.
European Journal of Human Genetics : EJHG
|
June 15, 2000
Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration
F Krämer, K White, D Pauleikhoff, et al.
Human Molecular Genetics
|
January 15, 1999
Characterization of ATM gene mutations in 66 ataxia telangiectasia families
N Sandoval, M Platzer, A Rosenthal, et al.
Neurology
|
September 17, 1999
DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland
F Laccone, U Engel, E Holinski-Feder, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 2, 1996
A high-resolution physical map of human chromosome 11
S Qin, N J Nowak, J Zhang, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 91) with videos related to
Sort By:
Page
of 10
American Journal of Human Genetics
|
August 26, 2000
A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration
A Rivera, K White, H Stöhr, et al.
Gynecologic Oncology
|
March 4, 1999
Frequency of BRCA1 mutation 5382insC in German breast cancer patients
J Backe, S Hofferbert, B Skawran, et al.
The British Journal of Ophthalmology
|
July 24, 2001
Evaluation of the G protein coupled receptor-75 (GPR75) in age related macular degeneration
C G Sauer, K White, H Stöhr, et al.
American Journal of Human Genetics
|
June 23, 1998
Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q
R E Kelsell, K Gregory-Evans, C Y Gregory-Evans, et al.
Genomics
|
April 15, 1997
A sequence-ready high-resolution physical map of the best macular dystrophy gene region in 11q12-q13
P R Cooper, N J Nowak, M J Higgins, et al.
Nature Genetics
|
July 14, 1998
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
T M Strom, G Nyakatura, E Apfelstedt-Sylla, et al.
European Journal of Human Genetics : EJHG
|
June 15, 2000
Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration
F Krämer, K White, D Pauleikhoff, et al.
Human Molecular Genetics
|
January 15, 1999
Characterization of ATM gene mutations in 66 ataxia telangiectasia families
N Sandoval, M Platzer, A Rosenthal, et al.
Neurology
|
September 17, 1999
DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland
F Laccone, U Engel, E Holinski-Feder, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 2, 1996
A high-resolution physical map of human chromosome 11
S Qin, N J Nowak, J Zhang, et al.
Page
of 10