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J Weissenbach

Showing results (181-190 of 363) with videos related to

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Human Genetics|August 1, 1987
Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesisF Waibel, G Scherer, M Fraccaro, et al.
British Journal of Cancer|November 1, 1995
Loss of heterozygosity in sporadic breast tumours at the BRCA2 locus on chromosome 13q12-q13A M Cleton-Jansen, N Collins, S R Lakhani, et al.
Annals of Human Genetics|October 1, 1995
Integrated genetic map of human chromosome 2S Cox, S P Bryant, A Collins, et al.
American Journal of Human Genetics|January 1, 1995
Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneityS Gispert, N Santos, R Damen, et al.
American Journal of Human Genetics|October 1, 1995
Refinement of the OPA1 gene locus on chromosome 3q28-q29 to a region of 2-8 cM, in one Cuban pedigree with autosomal dominant optic atrophy type KjerA Lunkes, U Hartung, C Magariño, et al.
Neurology|December 1, 1994
Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entitiesR Gouider, E LeGuern, J Emile, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1980
Two interferon mRNAs in human fibroblasts: in vitro translation and Escherichia coli cloning studiesJ Weissenbach, Y Chernajovsky, M Zeevi, et al.
Nature Genetics|October 1, 1994
Exclusion of HRAS from long QT locusN Roy, P Kahlem, E Dausse, et al.
Human Genetics|September 16, 1998
Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22J Fischer, J A Urtizberea, S Pavek, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1993
A 4.5-megabase yeast artificial chromosome contig from human chromosome 13q14.3 ordering 9 polymorphic microsatellites (22 sequence-tagged sites) tightly linked to the Wilson disease locusA White, J Tomfohrde, E Stewart, et al.
Pageof 37

Showing results (181-190 of 363) with videos related to

Sort By:
Pageof 37
Human Genetics|August 1, 1987
Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesisF Waibel, G Scherer, M Fraccaro, et al.
British Journal of Cancer|November 1, 1995
Loss of heterozygosity in sporadic breast tumours at the BRCA2 locus on chromosome 13q12-q13A M Cleton-Jansen, N Collins, S R Lakhani, et al.
Annals of Human Genetics|October 1, 1995
Integrated genetic map of human chromosome 2S Cox, S P Bryant, A Collins, et al.
American Journal of Human Genetics|January 1, 1995
Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneityS Gispert, N Santos, R Damen, et al.
American Journal of Human Genetics|October 1, 1995
Refinement of the OPA1 gene locus on chromosome 3q28-q29 to a region of 2-8 cM, in one Cuban pedigree with autosomal dominant optic atrophy type KjerA Lunkes, U Hartung, C Magariño, et al.
Neurology|December 1, 1994
Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entitiesR Gouider, E LeGuern, J Emile, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1980
Two interferon mRNAs in human fibroblasts: in vitro translation and Escherichia coli cloning studiesJ Weissenbach, Y Chernajovsky, M Zeevi, et al.
Nature Genetics|October 1, 1994
Exclusion of HRAS from long QT locusN Roy, P Kahlem, E Dausse, et al.
Human Genetics|September 16, 1998
Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22J Fischer, J A Urtizberea, S Pavek, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1993
A 4.5-megabase yeast artificial chromosome contig from human chromosome 13q14.3 ordering 9 polymorphic microsatellites (22 sequence-tagged sites) tightly linked to the Wilson disease locusA White, J Tomfohrde, E Stewart, et al.
Pageof 37