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Human Genetics|January 1, 1985
Mitotic chiasmata, gene density, and oncogenesE M Kuhn, E Therman, C DennistonHuman Genetics|January 1, 1985
Maternal age-specific rates of numerical chromosome abnormalities with special reference to trisomyT Hassold, D ChiuHuman Genetics|January 1, 1985
Homozygosity for the variant alpha-L-fucosidase trait and mucolipidosis IIIR Gatti, C Lombardo, P P CardoHuman Genetics|January 1, 1985
Height of females with pure gonadal dysgenesis and normal male or female karyotypeK BoczkowskiHuman Genetics|January 1, 1985
Deletion of band 13q21 is compatible with normal phenotypeJ Couturier, N Morichon-Delvallez, B DutrillauxHuman Genetics|September 22, 2022
Retrotransposon insertion as a novel mutational cause of spinal muscular atrophyMyriam Vezain, Christel Thauvin-Robinet, Yoann Vial, et al.Human Genetics|June 1, 1987
Genetic polymorphism of human plasma alpha 1B-glycoprotein: phenotyping by immunoblotting or by a simple method of 2-D electrophoresisB Gahne, R K Juneja, A StratilHuman Genetics|June 1, 1987
Three new G6PD variants, G6PD Adana, G6PD Samandağ, and G6PD Balcali in Cukurova, TurkeyK Aksoy, G T Yüregir, N Dikmen, et al.Human Genetics|October 1, 1986
Identity of the polymorphisms for esterase D and S-formylglutathione hydrolase in red blood cellsH Eiberg, J MohrHuman Genetics|October 1, 1986
Evidence that S-formylglutathione hydrolase and esterase D polymorphisms are identicalF Apeshiotis, K BenderPageof 958