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J Terwilliger

Showing results (11-20 of 24) with videos related to

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Hypertension (Dallas, Tex. : 1979)|March 19, 1999
Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertensionK Kainulainen, M Perola, J Terwilliger, et al.
Annals of Internal Medicine|June 1, 1993
United we standR M Glickman, J C Bennett, J P Nolan, et al.
Genomics|February 1, 1990
Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locusS P Kwan, J Terwilliger, R Parmley, et al.
Journal of the Neurological Sciences|April 1, 1991
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27M R Passos-Bueno, B Byth, D Love, et al.
Genetic Epidemiology|January 17, 2002
Evolution of the simulated data problemD C Thomas, I B Borecki, G Thomson, et al.
Nature Genetics|April 1, 1995
A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12qM Vaxillaire, V Boccio, A Philippi, et al.
American Journal of Human Genetics|February 1, 1992
Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysisK A Ellison, C P Fill, J Terwilliger, et al.
Journal of Experimental Botany|March 13, 2016
Changes and their possible causes in δ13C of dark-respired CO2 and its putative bulk and soluble sources during maize ontogenyJaleh Ghashghaie, Franz W Badeck, Cyril Girardin, et al.
Genomics|July 1, 1993
Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant retinitis pigmentosaS Bunge, H Wedemann, D David, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21P Paavola, T Heliö, M Kiuru, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Hypertension (Dallas, Tex. : 1979)|March 19, 1999
Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertensionK Kainulainen, M Perola, J Terwilliger, et al.
Annals of Internal Medicine|June 1, 1993
United we standR M Glickman, J C Bennett, J P Nolan, et al.
Genomics|February 1, 1990
Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locusS P Kwan, J Terwilliger, R Parmley, et al.
Journal of the Neurological Sciences|April 1, 1991
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27M R Passos-Bueno, B Byth, D Love, et al.
Genetic Epidemiology|January 17, 2002
Evolution of the simulated data problemD C Thomas, I B Borecki, G Thomson, et al.
Nature Genetics|April 1, 1995
A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12qM Vaxillaire, V Boccio, A Philippi, et al.
American Journal of Human Genetics|February 1, 1992
Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysisK A Ellison, C P Fill, J Terwilliger, et al.
Journal of Experimental Botany|March 13, 2016
Changes and their possible causes in δ13C of dark-respired CO2 and its putative bulk and soluble sources during maize ontogenyJaleh Ghashghaie, Franz W Badeck, Cyril Girardin, et al.
Genomics|July 1, 1993
Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant retinitis pigmentosaS Bunge, H Wedemann, D David, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21P Paavola, T Heliö, M Kiuru, et al.
Pageof 3