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Human heredity

Showing results (141-150 of 2,904) with videos related to

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Human Heredity|January 1, 1976
Blood group genetic studies in an urban Chinese populationB R Hawkins, M J Simons
Human Heredity|January 1, 1977
Nosologic groups. An overviewN Freire-Maia
Human Heredity|January 1, 1977
Genetics of asymmetry in dermatologlyphic traitsM P Mi, M N Rashad
Human Heredity|November 1, 1996
Quantitative genetics of dehydroepiandrosterone sulfate and its relation to possible cardiovascular disease risk factors in Mexican AmericansC E Jaquish, J Blangero, S M Haffner, et al.
Human Heredity|November 1, 1996
A novel mutation H373Y in the Wilms' tumor suppressor gene, WT1, associated with Denys-Drash syndromeM Ghahremani, C B Chan, T Bistritzer, et al.
Human Heredity|January 1, 1997
Three mutations in the paired homeodomain of PAX3 that cause Waardenburg syndrome type 1R Morell, M L Carey, A K Lalwani, et al.
Human Heredity|January 1, 1997
Prevalence of erythrocyte pyruvate kinase deficiency and normal values of enzyme in a Turkish populationH Akin, A Baykal-Erkiliç, A Aksu, et al.
Human Heredity|January 1, 1997
Identification of polymorphisms in the p53 gene by denaturing gradient gel blotsC P Nogueira
Human Heredity|May 1, 1997
Data on six short-tandem repeat polymorphisms in an autochthonous Basque populationM Iriondo, M C Barbero, N Izagirre, et al.
Human Heredity|May 1, 1997
Genotype-phenotype analysis in HbS-beta-thalassemiaC Altay, C Oner, R Oner, et al.
Pageof 291

Showing results (141-150 of 2,904) with videos related to

Sort By:
Pageof 291
Human Heredity|January 1, 1976
Blood group genetic studies in an urban Chinese populationB R Hawkins, M J Simons
Human Heredity|January 1, 1977
Nosologic groups. An overviewN Freire-Maia
Human Heredity|January 1, 1977
Genetics of asymmetry in dermatologlyphic traitsM P Mi, M N Rashad
Human Heredity|November 1, 1996
Quantitative genetics of dehydroepiandrosterone sulfate and its relation to possible cardiovascular disease risk factors in Mexican AmericansC E Jaquish, J Blangero, S M Haffner, et al.
Human Heredity|November 1, 1996
A novel mutation H373Y in the Wilms' tumor suppressor gene, WT1, associated with Denys-Drash syndromeM Ghahremani, C B Chan, T Bistritzer, et al.
Human Heredity|January 1, 1997
Three mutations in the paired homeodomain of PAX3 that cause Waardenburg syndrome type 1R Morell, M L Carey, A K Lalwani, et al.
Human Heredity|January 1, 1997
Prevalence of erythrocyte pyruvate kinase deficiency and normal values of enzyme in a Turkish populationH Akin, A Baykal-Erkiliç, A Aksu, et al.
Human Heredity|January 1, 1997
Identification of polymorphisms in the p53 gene by denaturing gradient gel blotsC P Nogueira
Human Heredity|May 1, 1997
Data on six short-tandem repeat polymorphisms in an autochthonous Basque populationM Iriondo, M C Barbero, N Izagirre, et al.
Human Heredity|May 1, 1997
Genotype-phenotype analysis in HbS-beta-thalassemiaC Altay, C Oner, R Oner, et al.
Pageof 291