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Human genetics

Showing results (1221-1230 of 9,569) with videos related to

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Human Genetics|October 1, 1988
Restriction endonuclease mapping of six novel deletions of the factor VIII gene in hemophilia AH Youssoufian, C K Kasper, D G Phillips, et al.
Human Genetics|October 1, 1989
A new familial syndrome with impaired function of three related peptide growth factorsH J Hoepffner, M Dreyer, U Reimers, et al.
Human Genetics|November 1, 1988
Detection of a rare-cutter RFLP in a CpG-rich island near the cystic fibrosis locusP Stanier, X Estivill, N Lench, et al.
Human Genetics|May 1, 1988
Molecular characterization of a Y;15 translocation segregating in a familyT Alitalo, J Tiihonen, P Hakola, et al.
Human Genetics|May 1, 1988
Replication kinetics of X chromosomes in fibroblasts and lymphocytesK S Reddy, J R Savage, D G Papworth
Human Genetics|May 1, 1988
G6PD Huntsville: a new glucose-6-phosphate dehydrogenase associated with chronic hemolytic anemiaK Hall, M T Schreeder, J T Prchal
Human Genetics|March 12, 2021
High-throughput STELA provides a rapid test for the diagnosis of telomere biology disordersKevin Norris, Amanda J Walne, Mark J Ponsford, et al.
Human Genetics|April 21, 2017
Loss of chromosome Y (LOY) in blood cells is associated with increased risk for disease and mortality in aging menLars A Forsberg
Human Genetics|February 1, 1988
Localization of the human G-CSF gene to the region of a breakpoint in the translocation typical of acute promyelocytic leukemiaR N Simmers, J Smith, M F Shannon, et al.
Human Genetics|February 25, 2014
CUBN and NEBL common variants in the chromosome 10p13 linkage region are associated with multibacillary leprosy in VietnamAudrey V Grant, Aurelie Cobat, Nguyen Van Thuc, et al.
Pageof 957

Showing results (1221-1230 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|October 1, 1988
Restriction endonuclease mapping of six novel deletions of the factor VIII gene in hemophilia AH Youssoufian, C K Kasper, D G Phillips, et al.
Human Genetics|October 1, 1989
A new familial syndrome with impaired function of three related peptide growth factorsH J Hoepffner, M Dreyer, U Reimers, et al.
Human Genetics|November 1, 1988
Detection of a rare-cutter RFLP in a CpG-rich island near the cystic fibrosis locusP Stanier, X Estivill, N Lench, et al.
Human Genetics|May 1, 1988
Molecular characterization of a Y;15 translocation segregating in a familyT Alitalo, J Tiihonen, P Hakola, et al.
Human Genetics|May 1, 1988
Replication kinetics of X chromosomes in fibroblasts and lymphocytesK S Reddy, J R Savage, D G Papworth
Human Genetics|May 1, 1988
G6PD Huntsville: a new glucose-6-phosphate dehydrogenase associated with chronic hemolytic anemiaK Hall, M T Schreeder, J T Prchal
Human Genetics|March 12, 2021
High-throughput STELA provides a rapid test for the diagnosis of telomere biology disordersKevin Norris, Amanda J Walne, Mark J Ponsford, et al.
Human Genetics|April 21, 2017
Loss of chromosome Y (LOY) in blood cells is associated with increased risk for disease and mortality in aging menLars A Forsberg
Human Genetics|February 1, 1988
Localization of the human G-CSF gene to the region of a breakpoint in the translocation typical of acute promyelocytic leukemiaR N Simmers, J Smith, M F Shannon, et al.
Human Genetics|February 25, 2014
CUBN and NEBL common variants in the chromosome 10p13 linkage region are associated with multibacillary leprosy in VietnamAudrey V Grant, Aurelie Cobat, Nguyen Van Thuc, et al.
Pageof 957