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Human Genetics|December 1, 1993
von Hippel-Lindau disease: identification of deletion mutations by pulsed-field gel electrophoresisM Yao, F Latif, M L Orcutt, et al.Human Genetics|February 26, 2010
The Q223R polymorphism in LEPR is associated with obesity in Pacific IslandersTakuro Furusawa, Izumi Naka, Taro Yamauchi, et al.Human Genetics|January 26, 2010
Selection and mutation in the "new" genetics: an emerging hypothesisBruce Gottlieb, Lenore K Beitel, Carlos Alvarado, et al.Human Genetics|January 1, 1984
Duchenne muscular dystrophy. Frequency of sporadic casesG A Danieli, G BarbujaniHuman Genetics|January 1, 1984
Considerations on the mechanism of differential Giemsa staining of BrdU-substituted chromosomesG SpeitHuman Genetics|April 1, 1993
Analysis of 160 CF chromosomes: detection of a novel mutation in exon 20I Dorval, S Odent, P Jezequel, et al.Human Genetics|April 1, 1993
Colocalization of the genes coding for the alpha 3 and beta 3 subunits of soluble guanylyl cyclase to human chromosome 4 at q31.3-q33G Giuili, N Roechel, U Scholl, et al.Human Genetics|April 1, 1993
An interleukin-8 (IL-8) cDNA clone identifies a frequent HindIII polymorphismM F Fey, A ToblerHuman Genetics|January 1, 1981
Comparison of mathematical models for the maternal age dependence of Down's syndrome ratesS H Lamson, E B HookPageof 957