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Human genetics

Showing results (631-640 of 11,264) with videos related to

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Human Genetics|November 1, 1990
Cloning of the breakpoints of a deletion associated with choroidermiaF P Cremers, F Brunsmann, W Berger, et al.
Human Genetics|November 1, 1990
Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in ItalyI Dianzani, M Devoto, C Camaschella, et al.
Human Genetics|November 1, 1990
The Na+/H+ antiporter: a "melt" polymorphism allows regional mapping to the short arm of chromosome 1C R Dudley, L A Giuffra, P Tippett, et al.
Human Genetics|December 1, 1990
BglII restriction fragment length polymorphisms at the human p53 gene locusU Masharani, D Wolf
Human Genetics|September 23, 2009
Variants in toll-like receptors 2 and 9 influence susceptibility to pulmonary tuberculosis in Caucasians, African-Americans, and West AfricansDigna Rosa Velez, Christian Wejse, Martin E Stryjewski, et al.
Human Genetics|October 1, 1990
Analysis of non-disjunction in sex chromosome tetrasomy and pentasomyT Hassold, D Pettay, K May, et al.
Human Genetics|September 1, 1990
First analysis of the F508 deletion in cystic fibrosis patients from the GDRK Grade, K Will, R Szibor, et al.
Human Genetics|September 1, 1990
Genotyping of the Spanish cystic fibrosis population at the delta F508 mutation site and RFLP linked lociB Jaume-Roig, B Simon-Bouy, A Taillandier, et al.
Human Genetics|September 1, 1990
The frequency of the delta F508 mutation on cystic fibrosis chromosomes in Israeli families: correlation to CF haplotypes in Jewish communities and ArabsI Lerer, S Cohen, M Chemke, et al.
Human Genetics|July 1, 1990
Linkage of aspartylglucosaminuria (AGU) to marker loci on the long arm of chromosome 4K Grön, P Aula, L Peltonen
Pageof 1,127

Showing results (631-640 of 11,264) with videos related to

Sort By:
Pageof 1,127
Human Genetics|November 1, 1990
Cloning of the breakpoints of a deletion associated with choroidermiaF P Cremers, F Brunsmann, W Berger, et al.
Human Genetics|November 1, 1990
Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in ItalyI Dianzani, M Devoto, C Camaschella, et al.
Human Genetics|November 1, 1990
The Na+/H+ antiporter: a "melt" polymorphism allows regional mapping to the short arm of chromosome 1C R Dudley, L A Giuffra, P Tippett, et al.
Human Genetics|December 1, 1990
BglII restriction fragment length polymorphisms at the human p53 gene locusU Masharani, D Wolf
Human Genetics|September 23, 2009
Variants in toll-like receptors 2 and 9 influence susceptibility to pulmonary tuberculosis in Caucasians, African-Americans, and West AfricansDigna Rosa Velez, Christian Wejse, Martin E Stryjewski, et al.
Human Genetics|October 1, 1990
Analysis of non-disjunction in sex chromosome tetrasomy and pentasomyT Hassold, D Pettay, K May, et al.
Human Genetics|September 1, 1990
First analysis of the F508 deletion in cystic fibrosis patients from the GDRK Grade, K Will, R Szibor, et al.
Human Genetics|September 1, 1990
Genotyping of the Spanish cystic fibrosis population at the delta F508 mutation site and RFLP linked lociB Jaume-Roig, B Simon-Bouy, A Taillandier, et al.
Human Genetics|September 1, 1990
The frequency of the delta F508 mutation on cystic fibrosis chromosomes in Israeli families: correlation to CF haplotypes in Jewish communities and ArabsI Lerer, S Cohen, M Chemke, et al.
Human Genetics|July 1, 1990
Linkage of aspartylglucosaminuria (AGU) to marker loci on the long arm of chromosome 4K Grön, P Aula, L Peltonen
Pageof 1,127