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Human genetics

Showing results (601-610 of 11,264) with videos related to

Pageof 1,127
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Human Genetics|October 21, 2010
Gene symbol: EDA. Disease: Ectodermal dysplasiaChiara Conte
Human Genetics|October 21, 2010
Gene symbol: CYP21A2. Disease: Adrenal hyperplasiaEttore Capoluongo, Paola Concolino, Francesca Vendittelli, et al.
Human Genetics|October 21, 2010
Gene symbol: MAP2K1. Disease: Cardio-Facio-Cutaneous syndromeHélène Cave
Human Genetics|October 21, 2010
Gene symbol: GNE. Disease: Inclusion body myopathyClaudio Bruno, M Grandis, D Cassandrini, et al.
Human Genetics|October 21, 2010
Gene symbol: HBD. Disease: Thalassaemia deltaChiara Refaldi, M D Cappellini
Human Genetics|June 9, 1978
Comparative studies in two cases of testicular feminization syndrome, one with and the other without the fluorescent distal band q12 of the YA Barbarino, A Serra, E Menini, et al.
Human Genetics|December 15, 2010
Potential involvement of more than one locus in trait manifestation for individuals with Leber congenital amaurosisWojciech Wiszniewski, Richard Alan Lewis, David W Stockton, et al.
Human Genetics|November 26, 2010
Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID populationCong Li, Fan Wang, Yanzong Yang, et al.
Human Genetics|May 1, 1990
Cocultivation of Fanconi anemia cells and of mouse lymphoma mutants leads to interspecies complementation of chromosomal hypersensitivity to DNA cross-linking agentsF Rosselli, E Moustacchi
Human Genetics|November 1, 1991
A rare insertional translocation of proximal segment with heterochromatic region of 1q into 7p in monozygotic twins and spontaneous abortionsR S Muneer, L M Thompson, E Kamat
Pageof 1,127

Showing results (601-610 of 11,264) with videos related to

Sort By:
Pageof 1,127
Human Genetics|October 21, 2010
Gene symbol: EDA. Disease: Ectodermal dysplasiaChiara Conte
Human Genetics|October 21, 2010
Gene symbol: CYP21A2. Disease: Adrenal hyperplasiaEttore Capoluongo, Paola Concolino, Francesca Vendittelli, et al.
Human Genetics|October 21, 2010
Gene symbol: MAP2K1. Disease: Cardio-Facio-Cutaneous syndromeHélène Cave
Human Genetics|October 21, 2010
Gene symbol: GNE. Disease: Inclusion body myopathyClaudio Bruno, M Grandis, D Cassandrini, et al.
Human Genetics|October 21, 2010
Gene symbol: HBD. Disease: Thalassaemia deltaChiara Refaldi, M D Cappellini
Human Genetics|June 9, 1978
Comparative studies in two cases of testicular feminization syndrome, one with and the other without the fluorescent distal band q12 of the YA Barbarino, A Serra, E Menini, et al.
Human Genetics|December 15, 2010
Potential involvement of more than one locus in trait manifestation for individuals with Leber congenital amaurosisWojciech Wiszniewski, Richard Alan Lewis, David W Stockton, et al.
Human Genetics|November 26, 2010
Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID populationCong Li, Fan Wang, Yanzong Yang, et al.
Human Genetics|May 1, 1990
Cocultivation of Fanconi anemia cells and of mouse lymphoma mutants leads to interspecies complementation of chromosomal hypersensitivity to DNA cross-linking agentsF Rosselli, E Moustacchi
Human Genetics|November 1, 1991
A rare insertional translocation of proximal segment with heterochromatic region of 1q into 7p in monozygotic twins and spontaneous abortionsR S Muneer, L M Thompson, E Kamat
Pageof 1,127