Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis.

Nakura, J; Miki, T; Ye, L; Mitsuda, N; Zhao, Y; Kihara, K; Yu, C E; Oshima, J; Fukuchi, K I; Wijsman, E M; Schellenberg, G D; Martin, G M; Murano, S i; Hashimoto, K; Fujiwara, Y; Ogihara, T

Nakura, J; Miki, T; Ye, L; Mitsuda, N; Zhao, Y; Kihara, K; Yu, C E; Oshima, J; Fukuchi, K I; Wijsman, E M; Schellenberg, G D; Martin, G M; Murano, S i; Hashimoto, K; Fujiwara, Y; Ogihara, T.

Affiliation

Nakura J; Department of Geriatric Medicine, Osaka University Medical School, Osaka, 565, Japan.

Genomics ; 36(1): 130-41, 1996 Aug 15.

Article in En | MEDLINE | ID: mdl-8812424

Subject(s)

Chromosome Mapping/methods; Chromosomes, Human, Pair 8/genetics; Homozygote; Werner Syndrome/genetics; Asian People/genetics; Consanguinity; Dinucleotide Repeats/genetics; Genes, Recessive/genetics; Genetic Markers; Heterozygote; Humans; Japan; White People/genetics

Search on Google

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Werner Syndrome / Chromosomes, Human, Pair 8 / Chromosome Mapping / Homozygote Limits: Humans Country/Region as subject: Asia Language: En Journal: Genomics Year: 1996 Document type: Article

Search on Google

XML

PubMed Links