Showing results (1991-2000 of 3,511) with videos related to
Sort By:
Pageof 352
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.Journal of Human Genetics|September 25, 1999
No association between atopic asthma and a coding variant of Fc epsilon R1 beta in a Japanese populationM Ishizawa, M Shibasaki, Y Yokouchi, et al.Journal of Human Genetics|August 3, 1999
EYA1 nonsense mutation in a Japanese branchio-oto-renal syndrome familyS Usami, S Abe, H Shinkawa, et al.Journal of Human Genetics|August 3, 1999
An NcoI polymorphism in the human complement component 7 (C7) geneT Horiuchi, H Nishizaka, H Tsukamoto, et al.Journal of Human Genetics|May 12, 2000
X-chromosome inactivation in the human trophoblast of early pregnancyS Uehara, M Tamura, M Nata, et al.Journal of Human Genetics|May 12, 2000
A Japanese propositus with D-- phenotype characterized by the deletion of both the RHCE gene and D1S80 locus situated in chromosome 1p and the existence of a new CE-D-CE hybrid geneH Okuda, H Fujiwara, T Omi, et al.Journal of Human Genetics|May 12, 2000
Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese populationH Iwasa, T Itoh, R Nagai, et al.Pageof 352