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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.Journal of Human Genetics|September 25, 1999
Polymorphic forms of the protein L-isoaspartate (D-aspartate) O-methyltransferase involved in the repair of age-damaged proteinsC G DeVry, S ClarkeJournal of Human Genetics|September 25, 1999
Spermatogenic ability is different among males in different Y chromosome lineageY Kuroki, T Iwamoto, J Lee, et al.Journal of Human Genetics|September 25, 1999
Transitional change in interaction between HIF-1 and HNF-4 in response to hypoxiaW Zhang, T Tsuchiya, Y YasukochiJournal of Human Genetics|September 25, 1999
Rapid mass screening method and counseling for the 1555A-->G mitochondrial mutationS Usami, S Abe, H Shinkawa, et al.Pageof 353