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Journal of Human Genetics|March 4, 2000
Mutation analysis of two Japanese patients with Fanconi-Bickel syndromeM Akagi, K Inui, S Nakajima, et al.Journal of Human Genetics|March 18, 2000
Novel mutations of the ATP7B gene in Japanese patients with Wilson diseaseY Kusuda, K Hamaguchi, T Mori, et al.Journal of Human Genetics|March 18, 2000
A novel nonsense mutation of the PEPD gene in a Japanese patient with prolidase deficiencyS Kikuchi, A Tanoue, F Endo, et al.Journal of Human Genetics|November 26, 1999
Chromosomal imbalances in adult T-cell leukemia revealed by comparative genomic hybridization: gains at 14q32 and 2p16-22 in cell linesY Ariyama, T Mori, T Shinomiya, et al.Journal of Human Genetics|November 26, 1999
A novel LDLR mutation, H190Y, in a Utah kindred with familial hypercholesterolemiaP N Hopkins, L L Wu, S H Stephenson, et al.Journal of Human Genetics|November 26, 1999
Molecular characterization of galactokinase deficiency in Japanese patientsM Asada, Y Okano, T Imamura, et al.Journal of Human Genetics|November 26, 1999
Cloning and characterization of the human UDP-N-acetylglucosamine: alpha-1,3-D-mannoside beta-1,4-N-acetylglucosaminyltransferase IV-homologue (hGnT-IV-H) geneT Furukawa, E M Youssef, T Yatsuoka, et al.Journal of Human Genetics|November 26, 1999
Novel polymorphisms in the upstream region of the human dopamine D4 receptor (DRD4) geneH Mitsuyasu, H Ozawa, Y Takeda, et al.Journal of Human Genetics|November 26, 1999
Dinucleotide repeat polymorphism in the third intron of the NRAMP2/DMT1 geneF Kishi, S Fujishima, M TabuchiJournal of Human Genetics|November 26, 1999
Novel variants in the promoter region of the CREB gene in schizophrenic patientsY Kawanishi, S Harada, H Tachikawa, et al.Pageof 352