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Human genetics

Showing results (1011-1020 of 9,569) with videos related to

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Human Genetics|March 1, 1992
Quantitative correlation between the residual activity of beta-hexosaminidase A and arylsulfatase A and the severity of the resulting lysosomal storage diseaseP Leinekugel, S Michel, E Conzelmann, et al.
Human Genetics|March 1, 1992
Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C geneC B Grundy, S Schulman, M Krawczak, et al.
Human Genetics|March 1, 1992
Characterization of two novel polymorphisms at the human parathyroid hormone gene locusJ E Mullersman, J J Shields, B K Saha
Human Genetics|March 1, 1992
Two intragenic polymorphisms of the APC-gene detected by PCR and enzymatic digestionC Kraus, W G Ballhausen
Human Genetics|April 1, 1992
Allotype distribution of human T cell receptor beta and gamma chain genes in Caucasians, Asians and Australian aborigines: relevance to chronic hepatitis BP Soeharso, K M Summers, W G Cooksley
Human Genetics|January 1, 1992
Estimating the stability of the proposed imprinted state of the fragile-X mutation when transmitted by femalesP J Follette, C D Laird
Human Genetics|July 27, 1976
On the origin of the supernumerary chromosome in autosomal trisomies--with special reference to Down's syndrome. A bias in tracing nondisjunction by chromosomal and biochemical polymorphismsU Langenbeck, I Hansmann, B Hinney, et al.
Human Genetics|August 1, 1992
Identification of a missense phenylketonuria mutation at codon 408 in ChineseC H Lin, K J Hsiao, T F Tsai, et al.
Human Genetics|August 1, 1992
A haplotype-linked four base pair deletion upstream of the A gamma globin gene coincides with decreased gene expressionC Beldjord, R Ducrocq, S Nadifi, et al.
Human Genetics|January 24, 2004
Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populationsDoron M Behar, Daniel Garrigan, Matthew E Kaplan, et al.
Pageof 957

Showing results (1011-1020 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|March 1, 1992
Quantitative correlation between the residual activity of beta-hexosaminidase A and arylsulfatase A and the severity of the resulting lysosomal storage diseaseP Leinekugel, S Michel, E Conzelmann, et al.
Human Genetics|March 1, 1992
Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C geneC B Grundy, S Schulman, M Krawczak, et al.
Human Genetics|March 1, 1992
Characterization of two novel polymorphisms at the human parathyroid hormone gene locusJ E Mullersman, J J Shields, B K Saha
Human Genetics|March 1, 1992
Two intragenic polymorphisms of the APC-gene detected by PCR and enzymatic digestionC Kraus, W G Ballhausen
Human Genetics|April 1, 1992
Allotype distribution of human T cell receptor beta and gamma chain genes in Caucasians, Asians and Australian aborigines: relevance to chronic hepatitis BP Soeharso, K M Summers, W G Cooksley
Human Genetics|January 1, 1992
Estimating the stability of the proposed imprinted state of the fragile-X mutation when transmitted by femalesP J Follette, C D Laird
Human Genetics|July 27, 1976
On the origin of the supernumerary chromosome in autosomal trisomies--with special reference to Down's syndrome. A bias in tracing nondisjunction by chromosomal and biochemical polymorphismsU Langenbeck, I Hansmann, B Hinney, et al.
Human Genetics|August 1, 1992
Identification of a missense phenylketonuria mutation at codon 408 in ChineseC H Lin, K J Hsiao, T F Tsai, et al.
Human Genetics|August 1, 1992
A haplotype-linked four base pair deletion upstream of the A gamma globin gene coincides with decreased gene expressionC Beldjord, R Ducrocq, S Nadifi, et al.
Human Genetics|January 24, 2004
Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populationsDoron M Behar, Daniel Garrigan, Matthew E Kaplan, et al.
Pageof 957