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M F Leppert

Showing results (1-10 of 49) with videos related to

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Epilepsia|January 1, 1990
Gene mapping and other tools for discoveryM F Leppert
Seminars in Neurology|March 15, 2000
Susceptibility genes in human epilepsyM F Leppert, N Singh
Annals of the New York Academy of Sciences|January 1, 1991
Human genetic mapping and inherited deafness syndromesM F Leppert, R A Lewis
American Journal of Human Genetics|July 1, 1993
Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneityH Heath, C E Jackson, B Otterud, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 5, 1994
Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1J German, A M Roe, M F Leppert, et al.
American Journal of Human Genetics|October 27, 1997
Recessive inheritance of obesity in familial non-insulin-dependent diabetes mellitus, and lack of linkage to nine candidate genesS J Hasstedt, M Hoffman, M F Leppert, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1992
Genetic linkage analysis in familial benign hypercalcemia using a candidate gene strategy. I. Studies in four familiesH Heath, M F Leppert, R P Lifton, et al.
Genes, Chromosomes & Cancer|December 18, 2001
Uncommon TGFBRI allele is not associated with increased susceptibility to colon cancerW S Samowitz, K Curtin, M F Leppert, et al.
Thrombosis and Haemostasis|December 22, 1999
Hereditary thrombophilia as a model for multigenic diseaseE G Bovill, S J Hasstedt, M F Leppert, et al.
The American Journal of Pathology|June 11, 1999
BAT-26 and BAT-40 instability in colorectal adenomas and carcinomas and germline polymorphismsW S Samowitz, M L Slattery, J D Potter, et al.
Pageof 5

Showing results (1-10 of 49) with videos related to

Sort By:
Pageof 5
Epilepsia|January 1, 1990
Gene mapping and other tools for discoveryM F Leppert
Seminars in Neurology|March 15, 2000
Susceptibility genes in human epilepsyM F Leppert, N Singh
Annals of the New York Academy of Sciences|January 1, 1991
Human genetic mapping and inherited deafness syndromesM F Leppert, R A Lewis
American Journal of Human Genetics|July 1, 1993
Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia: evidence for locus heterogeneityH Heath, C E Jackson, B Otterud, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 5, 1994
Bloom syndrome: an analysis of consanguineous families assigns the locus mutated to chromosome band 15q26.1J German, A M Roe, M F Leppert, et al.
American Journal of Human Genetics|October 27, 1997
Recessive inheritance of obesity in familial non-insulin-dependent diabetes mellitus, and lack of linkage to nine candidate genesS J Hasstedt, M Hoffman, M F Leppert, et al.
The Journal of Clinical Endocrinology and Metabolism|September 1, 1992
Genetic linkage analysis in familial benign hypercalcemia using a candidate gene strategy. I. Studies in four familiesH Heath, M F Leppert, R P Lifton, et al.
Genes, Chromosomes & Cancer|December 18, 2001
Uncommon TGFBRI allele is not associated with increased susceptibility to colon cancerW S Samowitz, K Curtin, M F Leppert, et al.
Thrombosis and Haemostasis|December 22, 1999
Hereditary thrombophilia as a model for multigenic diseaseE G Bovill, S J Hasstedt, M F Leppert, et al.
The American Journal of Pathology|June 11, 1999
BAT-26 and BAT-40 instability in colorectal adenomas and carcinomas and germline polymorphismsW S Samowitz, M L Slattery, J D Potter, et al.
Pageof 5