Search research articles
Contact Us
Filters
Showing results (51-60 of 99) with videos related to
Page
of 10
Sort By:
Nature
|
July 21, 1988
Mapping of mutation causing Friedreich's ataxia to human chromosome 9
S Chamberlain, J Shaw, A Rowland, et al.
Nature Genetics
|
February 1, 1997
Mapping of a major genetic modifier of embryonic lethality in TGF beta 1 knockout mice
M Bonyadi, S A Rusholme, F M Cousins, et al.
American Journal of Human Genetics
|
November 1, 1987
Exclusion of catalytic and regulatory subunits of cAMP-dependent protein kinase as candidate genes for the defect causing cystic fibrosis
P Scambler, O Oyen, B Wainwright, et al.
American Journal of Human Genetics
|
February 1, 1991
Association of Treacher Collins syndrome and translocation 6p21.31/16p13.11: exclusion of the locus from these candidate regions
M J Dixon, E Haan, E Baker, et al.
Human Molecular Genetics
|
September 16, 1998
Measured haplotype analysis of the angiotensin-I converting enzyme gene
B Keavney, C A McKenzie, J M Connell, et al.
American Journal of Human Genetics
|
April 1, 1989
Genetic homogeneity at the Friedreich ataxia locus on chromosome 9
S Chamberlain, J Shaw, J Wallis, et al.
American Journal of Human Genetics
|
December 1, 1995
Segregation and linkage analysis of serum angiotensin I-converting enzyme levels: evidence for two quantitative-trait loci
C A McKenzie, C Julier, T Forrester, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 17, 2001
Identification of multiple quantitative trait loci linked to prion disease incubation period in mice
S E Lloyd, O N Onwuazor, J A Beck, et al.
Nature
|
March 5, 1987
Linkage of an X-chromosome cleft palate gene
G E Moore, A Ivens, J Chambers, et al.
Nature
|
February 8, 1990
Localization of the malignant hyperthermia susceptibility locus to human chromosome 19q12-13.2
T V McCarthy, J M Healy, J J Heffron, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 99) with videos related to
Sort By:
Page
of 10
Nature
|
July 21, 1988
Mapping of mutation causing Friedreich's ataxia to human chromosome 9
S Chamberlain, J Shaw, A Rowland, et al.
Nature Genetics
|
February 1, 1997
Mapping of a major genetic modifier of embryonic lethality in TGF beta 1 knockout mice
M Bonyadi, S A Rusholme, F M Cousins, et al.
American Journal of Human Genetics
|
November 1, 1987
Exclusion of catalytic and regulatory subunits of cAMP-dependent protein kinase as candidate genes for the defect causing cystic fibrosis
P Scambler, O Oyen, B Wainwright, et al.
American Journal of Human Genetics
|
February 1, 1991
Association of Treacher Collins syndrome and translocation 6p21.31/16p13.11: exclusion of the locus from these candidate regions
M J Dixon, E Haan, E Baker, et al.
Human Molecular Genetics
|
September 16, 1998
Measured haplotype analysis of the angiotensin-I converting enzyme gene
B Keavney, C A McKenzie, J M Connell, et al.
American Journal of Human Genetics
|
April 1, 1989
Genetic homogeneity at the Friedreich ataxia locus on chromosome 9
S Chamberlain, J Shaw, J Wallis, et al.
American Journal of Human Genetics
|
December 1, 1995
Segregation and linkage analysis of serum angiotensin I-converting enzyme levels: evidence for two quantitative-trait loci
C A McKenzie, C Julier, T Forrester, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 17, 2001
Identification of multiple quantitative trait loci linked to prion disease incubation period in mice
S E Lloyd, O N Onwuazor, J A Beck, et al.
Nature
|
March 5, 1987
Linkage of an X-chromosome cleft palate gene
G E Moore, A Ivens, J Chambers, et al.
Nature
|
February 8, 1990
Localization of the malignant hyperthermia susceptibility locus to human chromosome 19q12-13.2
T V McCarthy, J M Healy, J J Heffron, et al.
Page
of 10