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Human Genetics|March 1, 1992
Complementation of a DNA repair deficiency in six human tumor cell lines by chromosome 11R Parshad, F M Price, M Oshimura, et al.Human Genetics|March 1, 1992
PKU mutations R408Q and F299C in Norway: haplotype associations, geographic distributions and phenotype characteristicsH G Eiken, K Stangeland, L Skjelkvåle, et al.Human Genetics|May 19, 1976
Partial and complete trisomy 9: delineation of a trisomy 9 syndromeG R Sutherland, R F Carter, L L MorrisHuman Genetics|May 19, 1976
Increased sister chromatid exchange events in the human late replicating XW Schnedl, W Pumberger, R Czaker, et al.Human Genetics|May 19, 1976
Tricho-rhino-phalangeal syndrome. The first case in JapanN Fukushima, M Anakura, S Arashima, et al.Human Genetics|May 19, 1976
Pathomorphological changes in an early spontaneous abortus with triploidy (69, XXX)V P Kulazenko, L G KulazenkoHuman Genetics|April 24, 2003
A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosisSandrine Haut, Michèle Brivet, Guy Touati, et al.Human Genetics|April 15, 1976
Origin of the extra chromosome no. 21 in Down's syndromeP Wagenbichler, W Killian, A Rett, et al.Human Genetics|July 29, 2003
Relationship between serum HDL-C levels and common genetic variants of the endothelial lipase gene in Japanese school-aged childrenKimiko Yamakawa-Kobayashi, Hisako Yanagi, Kazue Endo, et al.Human Genetics|April 1, 1992
Point mutations in the upstream region of the alpha-galactosidase A gene exon 6 in an atypical variant of Fabry diseaseS Ishii, H Sakuraba, Y SuzukiPageof 959