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M F Leppert

Showing results (21-30 of 49) with videos related to

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Experimental Hematology|September 5, 1998
Localization to chromosome 11 of a gene encoding a human minor histocompatibility antigenM I Gubarev, J C Jenkin, B E Otterrud, et al.
American Journal of Human Genetics|November 1, 1987
Etiological heterogeneity in X-linked spastic paraplegiaL D Keppen, M F Leppert, P O'Connell, et al.
American Journal of Human Genetics|September 1, 1986
A DNA probe for the LDL receptor gene is tightly linked to hypercholesterolemia in a pedigree with early coronary diseaseM F Leppert, S J Hasstedt, T Holm, et al.
Neuron|May 11, 1992
Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenitaL J Ptácek, A L George, R L Barchi, et al.
The American Journal of Cardiology|July 15, 1993
Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular geneticsR R Williams, S C Hunt, M C Schumacher, et al.
Journal of Immunology (Baltimore, Md. : 1950)|December 15, 1996
Localization to chromosome 22 of a gene encoding a human minor histocompatibility antigenM I Gubarev, J C Jenkin, M F Leppert, et al.
Cell|December 9, 1991
Identification of a mutation in the gene causing hyperkalemic periodic paralysisL J Ptácek, A L George, R C Griggs, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 14, 2000
Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus. The NHLBI Family Heart StudyH Coon, R H Myers, I B Borecki, et al.
Gastroenterology|October 19, 2001
The colon cancer burden of genetically defined hereditary nonpolyposis colon cancerW S Samowitz, K Curtin, H H Lin, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1996
Role of the beta 3-adrenergic receptor locus in obesity and noninsulin-dependent diabetes among members of Caucasian families with a diabetic sibling pairS C Elbein, M Hoffman, K Barrett, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
Experimental Hematology|September 5, 1998
Localization to chromosome 11 of a gene encoding a human minor histocompatibility antigenM I Gubarev, J C Jenkin, B E Otterrud, et al.
American Journal of Human Genetics|November 1, 1987
Etiological heterogeneity in X-linked spastic paraplegiaL D Keppen, M F Leppert, P O'Connell, et al.
American Journal of Human Genetics|September 1, 1986
A DNA probe for the LDL receptor gene is tightly linked to hypercholesterolemia in a pedigree with early coronary diseaseM F Leppert, S J Hasstedt, T Holm, et al.
Neuron|May 11, 1992
Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenitaL J Ptácek, A L George, R L Barchi, et al.
The American Journal of Cardiology|July 15, 1993
Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular geneticsR R Williams, S C Hunt, M C Schumacher, et al.
Journal of Immunology (Baltimore, Md. : 1950)|December 15, 1996
Localization to chromosome 22 of a gene encoding a human minor histocompatibility antigenM I Gubarev, J C Jenkin, M F Leppert, et al.
Cell|December 9, 1991
Identification of a mutation in the gene causing hyperkalemic periodic paralysisL J Ptácek, A L George, R C Griggs, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 14, 2000
Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus. The NHLBI Family Heart StudyH Coon, R H Myers, I B Borecki, et al.
Gastroenterology|October 19, 2001
The colon cancer burden of genetically defined hereditary nonpolyposis colon cancerW S Samowitz, K Curtin, H H Lin, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1996
Role of the beta 3-adrenergic receptor locus in obesity and noninsulin-dependent diabetes among members of Caucasian families with a diabetic sibling pairS C Elbein, M Hoffman, K Barrett, et al.
Pageof 5