Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Leppert

Showing results (51-60 of 315) with videos related to

Pageof 32
Sort By:
Nucleic Acids Research|January 11, 1991
D7S448 detects a HindIII polymorphism located in the centromere region of chromosome 7M Dean, C Stewart, A Perry, et al.
Lancet (London, England)|May 8, 1993
Genetic susceptibility in familial multiple sclerosis not linked to the myelin basic protein geneJ Rose, S Gerken, S Lynch, et al.
Advances in Neurology|January 1, 1992
Tourette symptoms in 161 related family membersW M McMahon, M Leppert, F Filloux, et al.
Annals of Neurology|September 1, 1991
Discordance of T-cell receptor beta-chain genes in familial multiple sclerosisS G Lynch, J W Rose, J H Petajan, et al.
American Journal of Human Genetics|September 1, 1995
Intermediate inheritance of Tourette syndrome, assuming assortative matingS J Hasstedt, M Leppert, F Filloux, et al.
Genomics|November 1, 1991
A de novo cystic fibrosis mutation: CGA (Arg) to TGA (stop) at codon 851 of the CFTR geneM B White, M Leppert, D Nielsen, et al.
Trends in Neurosciences|February 1, 1989
Mapping genes for manic-depression and schizophrenia with DNA markersW Byerley, C Mellon, P O'Connell, et al.
American Journal of Human Genetics|December 1, 1990
Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I)P F Chance, T D Bird, P O'Connell, et al.
Genomics|November 1, 1988
A mapped set of genetic markers for human chromosome 9M Lathrop, Y Nakamura, P O'Connell, et al.
Cytogenetics and Cell Genetics|January 1, 1993
The human endothelin-1 gene (EDN1) encoding a peptide with potent vasoactive properties maps distal to HLA on chromosome arm 6p in close linkage to D6S89M R Hoehe, H Ehrenreich, B Otterud, et al.
Pageof 32

Showing results (51-60 of 315) with videos related to

Sort By:
Pageof 32
Nucleic Acids Research|January 11, 1991
D7S448 detects a HindIII polymorphism located in the centromere region of chromosome 7M Dean, C Stewart, A Perry, et al.
Lancet (London, England)|May 8, 1993
Genetic susceptibility in familial multiple sclerosis not linked to the myelin basic protein geneJ Rose, S Gerken, S Lynch, et al.
Advances in Neurology|January 1, 1992
Tourette symptoms in 161 related family membersW M McMahon, M Leppert, F Filloux, et al.
Annals of Neurology|September 1, 1991
Discordance of T-cell receptor beta-chain genes in familial multiple sclerosisS G Lynch, J W Rose, J H Petajan, et al.
American Journal of Human Genetics|September 1, 1995
Intermediate inheritance of Tourette syndrome, assuming assortative matingS J Hasstedt, M Leppert, F Filloux, et al.
Genomics|November 1, 1991
A de novo cystic fibrosis mutation: CGA (Arg) to TGA (stop) at codon 851 of the CFTR geneM B White, M Leppert, D Nielsen, et al.
Trends in Neurosciences|February 1, 1989
Mapping genes for manic-depression and schizophrenia with DNA markersW Byerley, C Mellon, P O'Connell, et al.
American Journal of Human Genetics|December 1, 1990
Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I)P F Chance, T D Bird, P O'Connell, et al.
Genomics|November 1, 1988
A mapped set of genetic markers for human chromosome 9M Lathrop, Y Nakamura, P O'Connell, et al.
Cytogenetics and Cell Genetics|January 1, 1993
The human endothelin-1 gene (EDN1) encoding a peptide with potent vasoactive properties maps distal to HLA on chromosome arm 6p in close linkage to D6S89M R Hoehe, H Ehrenreich, B Otterud, et al.
Pageof 32