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Human genetics

Showing results (331-340 of 11,262) with videos related to

Pageof 1,127
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Human Genetics|December 16, 2022
Mate-pair genome sequencing reveals structural variants for idiopathic male infertilityZirui Dong, Jicheng Qian, Tracy Sze Man Law, et al.
Human Genetics|December 20, 2022
CLEC16A interacts with retromer and TRIM27, and its loss impairs endosomal trafficking and neurodevelopmentDaphne J Smits, Jordy Dekker, Rachel Schot, et al.
Human Genetics|July 20, 2023
Editorial for the Neurogenetics and Neurogenomics special issueElaine T Lim, Yingleong Chan
Human Genetics|January 1, 1985
Hereditary hepatic porphyria with delta aminolevulinate dehydrase deficiency: immunologic characterization of the non-catalytic enzymeH de Verneuil, M Doss, N Brusco, et al.
Human Genetics|July 24, 2024
Long non-coding RNAs: recent insights, remaining challenges, and exciting new directionsRebecca E Andersen
Human Genetics|January 1, 1983
NOR activity and satellite association patterns in a family carrying a doubly satellited markerC M Tuck, B L Bordson, M Varela
Human Genetics|January 1, 1983
Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphismP Wieacker, N Horn, P Pearson, et al.
Human Genetics|January 1, 1984
Regional localization of the human genes for S-adenosylhomocysteine hydrolase (cen----q131) and adenosine deaminase (q131----qter) on chromosome 20T Mohandas, R S Sparkes, E J Suh, et al.
Human Genetics|January 1, 1984
Transferrin subtypes and variants in Germany; further evidence for a Tf null alleleS Weidinger, H Cleve, F Schwarzfischer, et al.
Human Genetics|January 1, 1983
Chromosome anomalies in 136 couples with a history of recurrent abortionsU Diedrich, I Hansmann, D Janke, et al.
Pageof 1,127

Showing results (331-340 of 11,262) with videos related to

Sort By:
Pageof 1,127
Human Genetics|December 16, 2022
Mate-pair genome sequencing reveals structural variants for idiopathic male infertilityZirui Dong, Jicheng Qian, Tracy Sze Man Law, et al.
Human Genetics|December 20, 2022
CLEC16A interacts with retromer and TRIM27, and its loss impairs endosomal trafficking and neurodevelopmentDaphne J Smits, Jordy Dekker, Rachel Schot, et al.
Human Genetics|July 20, 2023
Editorial for the Neurogenetics and Neurogenomics special issueElaine T Lim, Yingleong Chan
Human Genetics|January 1, 1985
Hereditary hepatic porphyria with delta aminolevulinate dehydrase deficiency: immunologic characterization of the non-catalytic enzymeH de Verneuil, M Doss, N Brusco, et al.
Human Genetics|July 24, 2024
Long non-coding RNAs: recent insights, remaining challenges, and exciting new directionsRebecca E Andersen
Human Genetics|January 1, 1983
NOR activity and satellite association patterns in a family carrying a doubly satellited markerC M Tuck, B L Bordson, M Varela
Human Genetics|January 1, 1983
Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphismP Wieacker, N Horn, P Pearson, et al.
Human Genetics|January 1, 1984
Regional localization of the human genes for S-adenosylhomocysteine hydrolase (cen----q131) and adenosine deaminase (q131----qter) on chromosome 20T Mohandas, R S Sparkes, E J Suh, et al.
Human Genetics|January 1, 1984
Transferrin subtypes and variants in Germany; further evidence for a Tf null alleleS Weidinger, H Cleve, F Schwarzfischer, et al.
Human Genetics|January 1, 1983
Chromosome anomalies in 136 couples with a history of recurrent abortionsU Diedrich, I Hansmann, D Janke, et al.
Pageof 1,127