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Human genetics

Showing results (881-890 of 9,569) with videos related to

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Human Genetics|September 22, 1977
No evidence for linkage disequilibrium between Bf and GLO in African negroidsK Bender, G Mauff, H W Hitzeroth
Human Genetics|September 22, 1977
A rare adenosine deaminase allele (ADA6) in an Arab moslem village in IsraelS Nevo
Human Genetics|March 1, 1993
Molecular cytogenetic study of patients with Pallister-Killian syndromeM Larramendy, M Heiskanen, M Wessman, et al.
Human Genetics|March 1, 1993
A new human brain cDNA molecule: assignment to chromosome 11q21-q23.1 and description of two polymorphisms studied by the polymerase chain reactionS Lefebvre, J F Bureau, F Muscatelli, et al.
Human Genetics|March 1, 1993
Changes of telomere lengths in human intracranial tumoursP Nürnberg, G Thiel, F Weber, et al.
Human Genetics|March 1, 1993
Why are some genetic diseases common? Distinguishing selection from other processes by molecular analysis of globin gene variantsJ Flint, R M Harding, J B Clegg, et al.
Human Genetics|April 7, 1977
Partial trisomy 12p due to t(12;21)pat translocationB Biederman, P Bowen, C Robertson, et al.
Human Genetics|April 15, 1977
UV-light induced sister chromatid exchanges in xeroderma pigmentosum lymphocytesA D Schönwald, E Passarge
Human Genetics|February 1, 1996
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cellsA Massari, G Novelli, A Colosimo, et al.
Human Genetics|February 1, 1996
Mutations in the iduronate-2-sulfatase gene in five Norwegians with Hunter syndromeT C Olsen, H G Eiken, P M Knappskog, et al.
Pageof 957

Showing results (881-890 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|September 22, 1977
No evidence for linkage disequilibrium between Bf and GLO in African negroidsK Bender, G Mauff, H W Hitzeroth
Human Genetics|September 22, 1977
A rare adenosine deaminase allele (ADA6) in an Arab moslem village in IsraelS Nevo
Human Genetics|March 1, 1993
Molecular cytogenetic study of patients with Pallister-Killian syndromeM Larramendy, M Heiskanen, M Wessman, et al.
Human Genetics|March 1, 1993
A new human brain cDNA molecule: assignment to chromosome 11q21-q23.1 and description of two polymorphisms studied by the polymerase chain reactionS Lefebvre, J F Bureau, F Muscatelli, et al.
Human Genetics|March 1, 1993
Changes of telomere lengths in human intracranial tumoursP Nürnberg, G Thiel, F Weber, et al.
Human Genetics|March 1, 1993
Why are some genetic diseases common? Distinguishing selection from other processes by molecular analysis of globin gene variantsJ Flint, R M Harding, J B Clegg, et al.
Human Genetics|April 7, 1977
Partial trisomy 12p due to t(12;21)pat translocationB Biederman, P Bowen, C Robertson, et al.
Human Genetics|April 15, 1977
UV-light induced sister chromatid exchanges in xeroderma pigmentosum lymphocytesA D Schönwald, E Passarge
Human Genetics|February 1, 1996
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cellsA Massari, G Novelli, A Colosimo, et al.
Human Genetics|February 1, 1996
Mutations in the iduronate-2-sulfatase gene in five Norwegians with Hunter syndromeT C Olsen, H G Eiken, P M Knappskog, et al.
Pageof 957