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J Weissenbach

Showing results (141-150 of 363) with videos related to

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Human Genetics|April 1, 1995
Exclusion of the cone-specific alpha-subunit of the transducin gene in Stargardt's diseaseS Gerber, J M Rozet, D Bonneau, et al.
Cytogenetic and Genome Research|April 1, 2006
A SAGE approach to identifying novel trans-acting factors involved in the X inactivation processA Bourdet, C Ciaudo, L Zakin, et al.
Genomics|September 1, 1993
High-density genetic map of the BRCA1 region of chromosome 17q12-q21L A Anderson, L Friedman, S Osborne-Lawrence, et al.
American Journal of Human Genetics|March 21, 2000
A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34B Fontaine, C S Davoine, A Dürr, et al.
Genome Research|May 5, 2001
The complete genome sequence of the lactic acid bacterium Lactococcus lactis ssp. lactis IL1403A Bolotin, P Wincker, S Mauger, et al.
Nature Genetics|October 1, 1996
Genetic localization of a locus controlling the intensity of infection by Schistosoma mansoni on chromosome 5q31-q33S Marquet, L Abel, D Hillaire, et al.
Genomics|November 20, 1995
Identification and cloning in yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancerN Hoggard, Y Hey, B Brintnell, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
Mapping of Papillon-Lefevre syndrome to the chromosome 11q14 regionJ Fischer, C Blanchet-Bardon, J F Prud'homme, et al.
American Journal of Human Genetics|May 1, 1994
Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19M Kestilä, M Männikkö, C Holmberg, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 2, 2000
Assignation of highly polymorphic markers on a canine purebred pedigreeL Tiret, J L Kessler, S Bentolila, et al.
Pageof 37

Showing results (141-150 of 363) with videos related to

Sort By:
Pageof 37
Human Genetics|April 1, 1995
Exclusion of the cone-specific alpha-subunit of the transducin gene in Stargardt's diseaseS Gerber, J M Rozet, D Bonneau, et al.
Cytogenetic and Genome Research|April 1, 2006
A SAGE approach to identifying novel trans-acting factors involved in the X inactivation processA Bourdet, C Ciaudo, L Zakin, et al.
Genomics|September 1, 1993
High-density genetic map of the BRCA1 region of chromosome 17q12-q21L A Anderson, L Friedman, S Osborne-Lawrence, et al.
American Journal of Human Genetics|March 21, 2000
A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34B Fontaine, C S Davoine, A Dürr, et al.
Genome Research|May 5, 2001
The complete genome sequence of the lactic acid bacterium Lactococcus lactis ssp. lactis IL1403A Bolotin, P Wincker, S Mauger, et al.
Nature Genetics|October 1, 1996
Genetic localization of a locus controlling the intensity of infection by Schistosoma mansoni on chromosome 5q31-q33S Marquet, L Abel, D Hillaire, et al.
Genomics|November 20, 1995
Identification and cloning in yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancerN Hoggard, Y Hey, B Brintnell, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
Mapping of Papillon-Lefevre syndrome to the chromosome 11q14 regionJ Fischer, C Blanchet-Bardon, J F Prud'homme, et al.
American Journal of Human Genetics|May 1, 1994
Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19M Kestilä, M Männikkö, C Holmberg, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 2, 2000
Assignation of highly polymorphic markers on a canine purebred pedigreeL Tiret, J L Kessler, S Bentolila, et al.
Pageof 37