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American Journal of Human Genetics
|
April 16, 2002
Quantitative trait loci on chromosomes 1, 2, 3, 4, 8, 9, 11, 12, and 18 control variation in levels of T and B lymphocyte subpopulations
M A Hall, P J Norman, B Thiel, et al.
Nature Genetics
|
May 1, 1995
Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p
L G Gouw, C D Kaplan, J H Haines, et al.
American Journal of Human Genetics
|
January 1, 1995
Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q
J K Fink, C T Wu, S M Jones, et al.
Genomics
|
November 1, 1987
Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes
D C Page, K Bieker, L G Brown, et al.
American Journal of Human Genetics
|
July 1, 1996
Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q
J K Fink, S Rainer, J Wilkowski, et al.
Molecular Psychiatry
|
February 20, 2008
A high-density SNP genome-wide linkage scan in a large autism extended pedigree
K Allen-Brady, J Miller, N Matsunami, et al.
Genomics
|
May 1, 1993
The CEPH consortium linkage map of human chromosome 13
A M Bowcock, S C Gerken, R I Barnes, et al.
Genomics
|
November 1, 1992
Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortium
B J Keats, A A Todorov, L D Atwood, et al.
The New England Journal of Medicine
|
September 1, 1988
Genetic alterations during colorectal-tumor development
B Vogelstein, E R Fearon, S R Hamilton, et al.
Cancer Research
|
November 1, 1992
Nonlinkage of 16q markers to familial predisposition to Wilms' tumor
V Huff, A E Reeve, M Leppert, et al.
Page
of 32
Search research articles
Search
Showing results (291-300 of 315) with videos related to
Sort By:
Page
of 32
American Journal of Human Genetics
|
April 16, 2002
Quantitative trait loci on chromosomes 1, 2, 3, 4, 8, 9, 11, 12, and 18 control variation in levels of T and B lymphocyte subpopulations
M A Hall, P J Norman, B Thiel, et al.
Nature Genetics
|
May 1, 1995
Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p
L G Gouw, C D Kaplan, J H Haines, et al.
American Journal of Human Genetics
|
January 1, 1995
Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q
J K Fink, C T Wu, S M Jones, et al.
Genomics
|
November 1, 1987
Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes
D C Page, K Bieker, L G Brown, et al.
American Journal of Human Genetics
|
July 1, 1996
Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q
J K Fink, S Rainer, J Wilkowski, et al.
Molecular Psychiatry
|
February 20, 2008
A high-density SNP genome-wide linkage scan in a large autism extended pedigree
K Allen-Brady, J Miller, N Matsunami, et al.
Genomics
|
May 1, 1993
The CEPH consortium linkage map of human chromosome 13
A M Bowcock, S C Gerken, R I Barnes, et al.
Genomics
|
November 1, 1992
Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortium
B J Keats, A A Todorov, L D Atwood, et al.
The New England Journal of Medicine
|
September 1, 1988
Genetic alterations during colorectal-tumor development
B Vogelstein, E R Fearon, S R Hamilton, et al.
Cancer Research
|
November 1, 1992
Nonlinkage of 16q markers to familial predisposition to Wilms' tumor
V Huff, A E Reeve, M Leppert, et al.
Page
of 32