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Journal of Human Genetics|July 14, 2001
Linkage disequilibrium and haplotype analysis among eight novel single-nucleotide polymorphisms in the human tissue-type plasminogen activator (t-PA) geneI Nakazawa, T Nakajima, T Ishigami, et al.Journal of Human Genetics|July 14, 2001
Single nucleotide polymorphisms of RXRA encoding retinoid X receptor alphaR A Hegele, H CaoJournal of Human Genetics|June 8, 2001
Phenotypes of X-linked Charcot-Marie-Tooth disease and altered trafficking of mutant connexin 32 (GJB1)W Matsuyama, M Nakagawa, T Moritoyo, et al.Journal of Human Genetics|April 20, 2001
Construction of 700 human/mouse A9 monochromosomal hybrids and analysis of imprinted genes on human chromosome 6J Inoue, K Mitsuya, S Maegawa, et al.Journal of Human Genetics|April 20, 2001
Glycogen storage disease type Ia: molecular study in Brazilian patientsF de C Reis, H C Caldas, D Y Norato, et al.Journal of Human Genetics|April 20, 2001
Identification and allelic frequencies of novel single-nucleotide polymorphisms in the DUSP1 and BTG1 genesC Suzuki, M Unoki, Y NakamuraJournal of Human Genetics|April 20, 2001
Multiple single-nucleotide polymorphisms (SNPs) in the Japanese population in six candidate genes for long QT syndromeH Iwasa, M Kurabayashi, R Nagai, et al.Journal of Human Genetics|April 27, 2001
The c-Jun NH2-terminal kinase3 (JNK3) gene: genomic structure, chromosomal assignment, and loss of expression in brain tumorsS Yoshida, K Fukino, H Harada, et al.Journal of Human Genetics|April 27, 2001
Establishment of an optimized set of 406 microsatellite markers covering the whole genome for the Japanese populationK Ikari, H Onda, K Furushima, et al.Journal of Human Genetics|September 18, 2001
The hemoglobin O mutation in Indonesia: distribution and phenotypic expressionD Daud, A Harahap, I Setianingsih, et al.Pageof 353