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Journal of Human Genetics|August 15, 2001
Analysis of 168 short tandem repeat loci in the Japanese population, using a screening set for human genetic mappingM Mizutani, T Yamamoto, K Torii, et al.Journal of Human Genetics|August 15, 2001
Identification of sequence polymorphisms of the COMP (cartilage oligomeric matrix protein) gene and association study in osteoarthrosis of the knee and hip jointsA Mabuchi, T Ikeda, A Fukuda, et al.Journal of Human Genetics|September 18, 2001
High-density single-nucleotide polymorphism (SNP) map of the 150-kb region corresponding to the human ATP-binding cassette transporter A1 (ABCA1) geneA Iida, S Saito, A Sekine, et al.Journal of Human Genetics|September 18, 2001
Identification of sequence polymorphisms in two sulfation-related genes, PAPSS2 and SLC26A2, and an association analysis with knee osteoarthritisT Ikeda, A Mabuchi, A Fukuda, et al.Journal of Human Genetics|September 18, 2001
The T911C (F304S) substitution in the human ALG6 gene is a common polymorphism and not a causal mutation of CDG-IcS Vuillaumier-Barrot, C Le Bizec, G Durand, et al.Journal of Human Genetics|September 18, 2001
Single nucleotide polymorphisms of the resistin (RSTN) geneH Cao, R A HegeleJournal of Human Genetics|July 12, 2002
Homozygous deletion on the chromosomal region 5q12.3 in human lines of small-cell lung cancersKenji Tamura, Wataru Miwa, Tomoko Maruyama, et al.Journal of Human Genetics|July 12, 2002
Strategies for genome-wide association studies: optimization of study designs by the stepwise focusing methodAkira Saito, Naoyuki KamataniJournal of Human Genetics|July 12, 2002
Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseasesMasaji Tachikawa, Yoshitaka Nagai, Koichiro Nakamura, et al.Journal of Human Genetics|July 12, 2002
Double deletions and missense mutations in the first nucleotide-binding fold of the ATP-binding cassette transporter A1 ( ABCA1) gene in Japanese patients with Tangier diseaseZhigang Guo, Akihiro Inazu, Wenxin Yu, et al.Pageof 352