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Human genetics

Showing results (1001-1010 of 9,569) with videos related to

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Human Genetics|December 1, 1992
Bloom's syndrome. XVIII. Hypermutability at a tandem-repeat locusJ Groden, J German
Human Genetics|December 1, 1992
The intron 7 donor splice site transition: a second Tay-Sachs disease mutation in French CanadaP Hechtman, B Boulay, M De Braekeleer, et al.
Human Genetics|December 1, 1992
Chromosomal assignment and linkage analysis of the human glutathione S-transferase mu gene (GSTM1) using intron specific polymerase chain reactionS Zhong, C R Wolf, N K Spurr
Human Genetics|December 1, 1992
A single base pair polymorphism in the WT1 gene detected by single-strand conformation polymorphism analysisN Groves, P N Baird, A Hogg, et al.
Human Genetics|January 17, 2004
Genetics of parkin-linked diseaseAndrew B West, Nigel T Maidment
Human Genetics|November 1, 1992
A homozygous missense arginine to histidine substitution at position 482 of the beta-galactosidase in an Italian infantile GM1-gangliosidosis patientG Mosna, S Fattore, G Tubiello, et al.
Human Genetics|November 1, 1992
Molecular analysis of type I-A (tyrosinase negative) oculocutaneous albinismW S Oetting, R A King
Human Genetics|November 1, 1992
Mutations in the conserved domain of SRY are uncommon in XY gonadal dysgenesisE K Pivnick, S Wachtel, D Woods, et al.
Human Genetics|November 1, 1992
A family with X-linked deafness showing linkage to the proximal Xq region of the X chromosomeD Robinson, M Lamont, G Curtis, et al.
Human Genetics|February 1, 1992
The Wiskott-Aldrich syndrome: refinement of the localization on Xp and identification of another closely linked marker locus, OATL1W L Greer, M Peacocke, K A Siminovitch
Pageof 957

Showing results (1001-1010 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|December 1, 1992
Bloom's syndrome. XVIII. Hypermutability at a tandem-repeat locusJ Groden, J German
Human Genetics|December 1, 1992
The intron 7 donor splice site transition: a second Tay-Sachs disease mutation in French CanadaP Hechtman, B Boulay, M De Braekeleer, et al.
Human Genetics|December 1, 1992
Chromosomal assignment and linkage analysis of the human glutathione S-transferase mu gene (GSTM1) using intron specific polymerase chain reactionS Zhong, C R Wolf, N K Spurr
Human Genetics|December 1, 1992
A single base pair polymorphism in the WT1 gene detected by single-strand conformation polymorphism analysisN Groves, P N Baird, A Hogg, et al.
Human Genetics|January 17, 2004
Genetics of parkin-linked diseaseAndrew B West, Nigel T Maidment
Human Genetics|November 1, 1992
A homozygous missense arginine to histidine substitution at position 482 of the beta-galactosidase in an Italian infantile GM1-gangliosidosis patientG Mosna, S Fattore, G Tubiello, et al.
Human Genetics|November 1, 1992
Molecular analysis of type I-A (tyrosinase negative) oculocutaneous albinismW S Oetting, R A King
Human Genetics|November 1, 1992
Mutations in the conserved domain of SRY are uncommon in XY gonadal dysgenesisE K Pivnick, S Wachtel, D Woods, et al.
Human Genetics|November 1, 1992
A family with X-linked deafness showing linkage to the proximal Xq region of the X chromosomeD Robinson, M Lamont, G Curtis, et al.
Human Genetics|February 1, 1992
The Wiskott-Aldrich syndrome: refinement of the localization on Xp and identification of another closely linked marker locus, OATL1W L Greer, M Peacocke, K A Siminovitch
Pageof 957