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Human Genetics|June 1, 1989
A rapid method for detection of Y-chromosomal DNA from dried blood specimens by the polymerase chain reactionM Witt, R P EricksonHuman Genetics|June 1, 1989
Dicarboxylic aminoaciduria associated with mental retardationM Swarna, D N Rao, P P ReddyHuman Genetics|August 1, 1989
BamHI and SacI RFLPs of the human immunoglobulin IGHG genes with reference to the Gm polymorphism in African people. Evidence for a major polymorphismN Ghanem, M Bensmana, J M Dugoujon, et al.Human Genetics|August 1, 1989
Detection of an unbalanced translocation (4;14) in a mildly retarded father and son by flow cytometryA Cooke, J L Tolmie, J M Colgan, et al.Human Genetics|September 1, 1989
RFLP-discordance within the human phenylalanine hydroxylase locusO Riess, A Michel, W Berger, et al.Human Genetics|April 1, 1989
Mapping of the gene encoding the multifunctional protein carrying out the first three steps of pyrimidine biosynthesis to human chromosome 2K C Chen, D B Vannais, C Jones, et al.Human Genetics|April 1, 1989
Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implicationsC Hohenschutz, P Eich, W Friedl, et al.Human Genetics|June 12, 2014
The population genomic landscape of human genetic structure, admixture history and local adaptation in Peninsular MalaysiaLian Deng, Boon Peng Hoh, Dongsheng Lu, et al.Human Genetics|March 1, 1989
Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on XpA Gal, A Schinzel, U Orth, et al.Human Genetics|March 1, 1989
Rapid isolation of moderate and highly polymorphic DNA fragments mapping close to WT (Wilms' tumour) and AN2 (aniridia) on chromosome 11P A Boyd, S Christie, N D Hastie, et al.Pageof 958