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Human heredity

Showing results (11-20 of 2,904) with videos related to

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Human Heredity|May 9, 2000
A novel Q562X mutation identified in the hMLH1 gene in a Slovenian patient with hereditary nonpolyposis colorectal cancerU Potocnik, D Glavac, R Golouh, et al.
Human Heredity|April 27, 2000
The 677 C-->T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in five Chinese ethnic groupsJ Yu, B Chen, G Zhang, et al.
Human Heredity|May 19, 2001
Optimal sibship selection for genotyping in quantitative trait locus linkage analysisS Purcell, S S Cherny, J K Hewitt, et al.
Human Heredity|May 19, 2001
A novel nonsense mutation of the GTP cyclohydrolase I gene in a family with dopa-responsive dystoniaK M Hong, Y S Kim, M K Paik
Human Heredity|July 19, 2000
Evidence for a founder effect in Sicilian patients with glycogen storage disease type IIF Dagnino, M Stroppiano, S Regis, et al.
Human Heredity|July 19, 2000
A complete enumeration and classification of two-locus disease modelsW Li, J Reich
Human Heredity|July 19, 2000
Haptoglobin phenotypes in HIV-1-seropositive patients in Ghana: decreased risk for Hp0 individualsI K Quaye, F A Ekuban, J A Brandful, et al.
Human Heredity|January 1, 1975
Phosphoglucomutase phenotypes and prenatal selection. Studies of spontaneous and induced abortionsG Beckman, L Beckman
Human Heredity|October 6, 2001
Y chromosome binary markers to study the high prevalence of males in Sardinian centenarians and the genetic structure of the Sardinian populationG Passarino, P A Underhill, L L Cavalli-Sforza, et al.
Human Heredity|October 6, 2001
Estimation of the heritability of latent variables which are included in a structural model for metabolic syndromeR Koch, U Julius, W Jaross, et al.
Pageof 291

Showing results (11-20 of 2,904) with videos related to

Sort By:
Pageof 291
Human Heredity|May 9, 2000
A novel Q562X mutation identified in the hMLH1 gene in a Slovenian patient with hereditary nonpolyposis colorectal cancerU Potocnik, D Glavac, R Golouh, et al.
Human Heredity|April 27, 2000
The 677 C-->T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in five Chinese ethnic groupsJ Yu, B Chen, G Zhang, et al.
Human Heredity|May 19, 2001
Optimal sibship selection for genotyping in quantitative trait locus linkage analysisS Purcell, S S Cherny, J K Hewitt, et al.
Human Heredity|May 19, 2001
A novel nonsense mutation of the GTP cyclohydrolase I gene in a family with dopa-responsive dystoniaK M Hong, Y S Kim, M K Paik
Human Heredity|July 19, 2000
Evidence for a founder effect in Sicilian patients with glycogen storage disease type IIF Dagnino, M Stroppiano, S Regis, et al.
Human Heredity|July 19, 2000
A complete enumeration and classification of two-locus disease modelsW Li, J Reich
Human Heredity|July 19, 2000
Haptoglobin phenotypes in HIV-1-seropositive patients in Ghana: decreased risk for Hp0 individualsI K Quaye, F A Ekuban, J A Brandful, et al.
Human Heredity|January 1, 1975
Phosphoglucomutase phenotypes and prenatal selection. Studies of spontaneous and induced abortionsG Beckman, L Beckman
Human Heredity|October 6, 2001
Y chromosome binary markers to study the high prevalence of males in Sardinian centenarians and the genetic structure of the Sardinian populationG Passarino, P A Underhill, L L Cavalli-Sforza, et al.
Human Heredity|October 6, 2001
Estimation of the heritability of latent variables which are included in a structural model for metabolic syndromeR Koch, U Julius, W Jaross, et al.
Pageof 291