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Human genetics

Showing results (1071-1080 of 9,569) with videos related to

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Human Genetics|April 1, 1995
An apolipoprotein CIII marker associated with hypertriglyceridemia in Caucasians also confers increased risk in a west Japanese populationQ Zeng, M Dammerman, Y Takada, et al.
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.
Human Genetics|April 1, 1995
Polymorphisms in the human DNA polymerase beta geneY Dobashi, Y Kubota, T Shuin, et al.
Human Genetics|April 1, 1995
New polymorphisms and markers in the HLA class I region: relevance to hereditary hemochromatosis (HFE)A Totaro, A Grifa, A Roetto, et al.
Human Genetics|April 1, 1995
A high-density microsatellite map of the ataxia-telangiectasia locusL Vanagaite, M R James, G Rotman, et al.
Human Genetics|February 1, 1995
Trisomy 7 in non-neoplastic tubular epithelial cells of the kidneyS Knuutila, M L Larramendy, P Elfving, et al.
Human Genetics|February 1, 1995
The PKU mutation S349P causes complete loss of catalytic activity in the recombinant phenylalanine hydroxylase enzymeP M Knappskog, H G Eiken, A Martinez, et al.
Human Genetics|February 1, 1995
Factor XKetchikan: a variant molecule in which Gly replaces a Gla residue at position 14 in the light chainD J Kim, A R Thompson, H L James
Human Genetics|February 1, 1995
Regional localization of the human EGF-like growth factor CRIPTO gene (TDGF-1) to chromosome 3p21S Saccone, A Rapisarda, S Motta, et al.
Human Genetics|June 1, 1995
Assignment of the gene responsible for cystinuria (rBAT) and of markers D2S119 and D2S177 to 2p16 by fluorescence in situ hybridizationM J Calonge, M Nadal, S Calvano, et al.
Pageof 957

Showing results (1071-1080 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|April 1, 1995
An apolipoprotein CIII marker associated with hypertriglyceridemia in Caucasians also confers increased risk in a west Japanese populationQ Zeng, M Dammerman, Y Takada, et al.
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.
Human Genetics|April 1, 1995
Polymorphisms in the human DNA polymerase beta geneY Dobashi, Y Kubota, T Shuin, et al.
Human Genetics|April 1, 1995
New polymorphisms and markers in the HLA class I region: relevance to hereditary hemochromatosis (HFE)A Totaro, A Grifa, A Roetto, et al.
Human Genetics|April 1, 1995
A high-density microsatellite map of the ataxia-telangiectasia locusL Vanagaite, M R James, G Rotman, et al.
Human Genetics|February 1, 1995
Trisomy 7 in non-neoplastic tubular epithelial cells of the kidneyS Knuutila, M L Larramendy, P Elfving, et al.
Human Genetics|February 1, 1995
The PKU mutation S349P causes complete loss of catalytic activity in the recombinant phenylalanine hydroxylase enzymeP M Knappskog, H G Eiken, A Martinez, et al.
Human Genetics|February 1, 1995
Factor XKetchikan: a variant molecule in which Gly replaces a Gla residue at position 14 in the light chainD J Kim, A R Thompson, H L James
Human Genetics|February 1, 1995
Regional localization of the human EGF-like growth factor CRIPTO gene (TDGF-1) to chromosome 3p21S Saccone, A Rapisarda, S Motta, et al.
Human Genetics|June 1, 1995
Assignment of the gene responsible for cystinuria (rBAT) and of markers D2S119 and D2S177 to 2p16 by fluorescence in situ hybridizationM J Calonge, M Nadal, S Calvano, et al.
Pageof 957