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Human Genetics|October 1, 1987
Molecular cloning of a pair of human pepsinogen A genes which differ by a Glu----Lys mutation in the activation peptideM P Evers, B Zelle, D S Peeper, et al.Human Genetics|January 1, 1985
Gene localisation of the PGM1 enzyme system and the Duffy blood groups on chromosome No. 1 by means of a new fragile site at 1p31J Herbich, J Szilvassy, W SchnedlHuman Genetics|June 1, 1987
The gene coding for the human T-lymphocyte CD2 antigen is located on chromosome 1pM H Brown, P A Gorman, W A Sewell, et al.Human Genetics|March 1, 1987
Ataxia-telangiectasia: an inherited disorder of ionizing-radiation sensitivity in man. Progress in the elucidation of the underlying biochemical defectP J McKinnonHuman Genetics|September 1, 1986
The evolution of the alpha- and beta-globin gene clusters in human populationsA V Hill, J S WainscoatHuman Genetics|October 12, 2021
How to fix a broken protein: restoring function to mutant human cystathionine β-synthaseWarren D KrugerHuman Genetics|October 13, 2021
WDR37 syndrome: identification of a distinct new cluster of disease-associated variants and functional analyses of mutant proteinsElena A Sorokina, Linda M Reis, Samuel Thompson, et al.Human Genetics|October 13, 2021
The population genetics characteristics of a 90 locus panel of microhaplotypesAndrew J Pakstis, Neeru Gandotra, William C Speed, et al.Human Genetics|October 1, 1986
Regional localisation of X chromosome short arm probesK Paulsen, S Forrest, G Scherer, et al.Human Genetics|October 1, 1986
Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome)K D MacDermot, R M Winter, S MalcolmPageof 959