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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.Journal of Human Genetics|May 12, 2000
Disparity between association and linkage analysis for HNF1A G319S in type 2 diabetes in Canadian Oji-CreeR A Hegele, A J Hanley, B Zinman, et al.Journal of Human Genetics|May 12, 2000
Molecular cloning and expression analysis of the human DA41 gene and its mapping to chromosome 9q21.2-q21.3E Hanaoka, T Ozaki, M Ohira, et al.Journal of Human Genetics|May 13, 1999
Molecular characterization of 6-pyruvoyl-tetrahydropterin synthase deficiency in Japanese patientsT Imamura, Y Okano, H Shintaku, et al.Journal of Human Genetics|May 13, 1999
Germline mutations of E-cadherin gene in Korean familial gastric cancer patientsK A Yoon, J L Ku, H K Yang, et al.Pageof 353