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Human genetics

Showing results (1051-1060 of 9,569) with videos related to

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Human Genetics|October 22, 2003
Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainmentFrance Gagnon, Gail P Jarvik, Arno G Motulsky, et al.
Human Genetics|September 27, 2003
No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approachJohannes Schumacher, Andreas C J Otte, Tim Becker, et al.
Human Genetics|January 28, 2004
Common variants within the interleukin 4 receptor alpha gene (IL4R) are associated with susceptibility to osteoarthritisTracy Forster, Kay Chapman, John Loughlin
Human Genetics|February 10, 2004
New clues on the origin of the Friedreich ataxia expanded alleles from the analysis of new polymorphisms closely linked to the mutationAntonella Monticelli, Manuela Giacchetti, Irene De Biase, et al.
Human Genetics|August 4, 2004
Genomic rearrangements at the IGHMBP2 gene locus in two patients with SMARD1Ulf P Guenther, Markus Schuelke, Enrico Bertini, et al.
Human Genetics|August 4, 2004
Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping arrayXiaofeng Zhou, Samuel C Mok, Zugen Chen, et al.
Human Genetics|December 29, 1978
Unstable telocentric chromosome produced after centric misdivision of a 21q/21q translocated elementG Guanti, F Maritato
Human Genetics|May 13, 2004
Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analysesKaren E Deffenbacher, Judith B Kenyon, Denise M Hoover, et al.
Human Genetics|June 29, 2004
A resistin gene polymorphism is associated with body mass index in womenVanessa S Mattevi, Verônica M Zembrzuski, Mara H Hutz
Human Genetics|June 29, 2004
Nemaline myopathy in the Ashkenazi Jewish population is caused by a deletion in the nebulin geneSylvia L Anderson, Josef Ekstein, Mary C Donnelly, et al.
Pageof 957

Showing results (1051-1060 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|October 22, 2003
Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainmentFrance Gagnon, Gail P Jarvik, Arno G Motulsky, et al.
Human Genetics|September 27, 2003
No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approachJohannes Schumacher, Andreas C J Otte, Tim Becker, et al.
Human Genetics|January 28, 2004
Common variants within the interleukin 4 receptor alpha gene (IL4R) are associated with susceptibility to osteoarthritisTracy Forster, Kay Chapman, John Loughlin
Human Genetics|February 10, 2004
New clues on the origin of the Friedreich ataxia expanded alleles from the analysis of new polymorphisms closely linked to the mutationAntonella Monticelli, Manuela Giacchetti, Irene De Biase, et al.
Human Genetics|August 4, 2004
Genomic rearrangements at the IGHMBP2 gene locus in two patients with SMARD1Ulf P Guenther, Markus Schuelke, Enrico Bertini, et al.
Human Genetics|August 4, 2004
Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping arrayXiaofeng Zhou, Samuel C Mok, Zugen Chen, et al.
Human Genetics|December 29, 1978
Unstable telocentric chromosome produced after centric misdivision of a 21q/21q translocated elementG Guanti, F Maritato
Human Genetics|May 13, 2004
Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analysesKaren E Deffenbacher, Judith B Kenyon, Denise M Hoover, et al.
Human Genetics|June 29, 2004
A resistin gene polymorphism is associated with body mass index in womenVanessa S Mattevi, Verônica M Zembrzuski, Mara H Hutz
Human Genetics|June 29, 2004
Nemaline myopathy in the Ashkenazi Jewish population is caused by a deletion in the nebulin geneSylvia L Anderson, Josef Ekstein, Mary C Donnelly, et al.
Pageof 957