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M Farrall

Showing results (51-60 of 99) with videos related to

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Nature|July 21, 1988
Mapping of mutation causing Friedreich's ataxia to human chromosome 9S 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 miceM 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 fibrosisP 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 regionsM J Dixon, E Haan, E Baker, et al.
Human Molecular Genetics|September 16, 1998
Measured haplotype analysis of the angiotensin-I converting enzyme geneB 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 9S 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 lociC 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 miceS E Lloyd, O N Onwuazor, J A Beck, et al.
Nature|March 5, 1987
Linkage of an X-chromosome cleft palate geneG E Moore, A Ivens, J Chambers, et al.
Nature|February 8, 1990
Localization of the malignant hyperthermia susceptibility locus to human chromosome 19q12-13.2T V McCarthy, J M Healy, J J Heffron, et al.
Pageof 10

Showing results (51-60 of 99) with videos related to

Sort By:
Pageof 10
Nature|July 21, 1988
Mapping of mutation causing Friedreich's ataxia to human chromosome 9S 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 miceM 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 fibrosisP 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 regionsM J Dixon, E Haan, E Baker, et al.
Human Molecular Genetics|September 16, 1998
Measured haplotype analysis of the angiotensin-I converting enzyme geneB 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 9S 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 lociC 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 miceS E Lloyd, O N Onwuazor, J A Beck, et al.
Nature|March 5, 1987
Linkage of an X-chromosome cleft palate geneG E Moore, A Ivens, J Chambers, et al.
Nature|February 8, 1990
Localization of the malignant hyperthermia susceptibility locus to human chromosome 19q12-13.2T V McCarthy, J M Healy, J J Heffron, et al.
Pageof 10