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Human genetics

Showing results (941-950 of 9,569) with videos related to

Pageof 957
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Human Genetics|March 1, 1996
Angelman syndrome in an inbred familyJ Beuten, R C Hennekam, B Van Roy, et al.
Human Genetics|March 1, 1996
The heritability of human longevity: a population-based study of 2872 Danish twin pairs born 1870-1900A M Herskind, M McGue, N V Holm, et al.
Human Genetics|March 1, 1996
A deletion of five nucleotides in the L1CAM gene in a Japanese family with X-linked hydrocephalusT Takechi, J Tohyama, T Kurashige, et al.
Human Genetics|March 1, 1996
No mutations found by RET mutation scanning in sporadic and hereditary neuroblastomaR M Hofstra, N C Cheng, C Hansen, et al.
Human Genetics|March 1, 1996
Most cases of medium-chain acyl-CoA dehydrogenase deficiency escape detection in FranceB Fromenty, A Mansouri, J P Bonnefont, et al.
Human Genetics|October 1, 1996
Novel polymorphisms and haplotypes in the human coagulation factor XIII A-subunit geneK Suzuki, J Henke, M Iwata, et al.
Human Genetics|October 1, 1996
Molecular analysis of the cystinuria disease gene: identification of four new mutations, one large deletion, and one polymorphismL Bisceglia, M J Calonge, L Dello Strologo, et al.
Human Genetics|October 1, 1996
Mutation analysis reveals an insertional hotspot in exon 4 of the LDL receptor geneM J Kotze, R Thiart, O Loubser, et al.
Human Genetics|November 7, 2016
The Y chromosome as the most popular marker in genetic genealogy benefits interdisciplinary researchFrancesc Calafell, Maarten H D Larmuseau
Human Genetics|January 1, 1989
Ataxia-telangiectasia fibroblasts have less fibronectin mRNA than control cells but have the same levels of integrin and beta-actin mRNAY Becker, E Tabor, Y Asher
Pageof 957

Showing results (941-950 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|March 1, 1996
Angelman syndrome in an inbred familyJ Beuten, R C Hennekam, B Van Roy, et al.
Human Genetics|March 1, 1996
The heritability of human longevity: a population-based study of 2872 Danish twin pairs born 1870-1900A M Herskind, M McGue, N V Holm, et al.
Human Genetics|March 1, 1996
A deletion of five nucleotides in the L1CAM gene in a Japanese family with X-linked hydrocephalusT Takechi, J Tohyama, T Kurashige, et al.
Human Genetics|March 1, 1996
No mutations found by RET mutation scanning in sporadic and hereditary neuroblastomaR M Hofstra, N C Cheng, C Hansen, et al.
Human Genetics|March 1, 1996
Most cases of medium-chain acyl-CoA dehydrogenase deficiency escape detection in FranceB Fromenty, A Mansouri, J P Bonnefont, et al.
Human Genetics|October 1, 1996
Novel polymorphisms and haplotypes in the human coagulation factor XIII A-subunit geneK Suzuki, J Henke, M Iwata, et al.
Human Genetics|October 1, 1996
Molecular analysis of the cystinuria disease gene: identification of four new mutations, one large deletion, and one polymorphismL Bisceglia, M J Calonge, L Dello Strologo, et al.
Human Genetics|October 1, 1996
Mutation analysis reveals an insertional hotspot in exon 4 of the LDL receptor geneM J Kotze, R Thiart, O Loubser, et al.
Human Genetics|November 7, 2016
The Y chromosome as the most popular marker in genetic genealogy benefits interdisciplinary researchFrancesc Calafell, Maarten H D Larmuseau
Human Genetics|January 1, 1989
Ataxia-telangiectasia fibroblasts have less fibronectin mRNA than control cells but have the same levels of integrin and beta-actin mRNAY Becker, E Tabor, Y Asher
Pageof 957