Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: Lessons learned from analysis of 35 chromosome 8p11.1-21.1 Markers

American Journal of Human Genetics

Volumn 58, Issue 6, 1996, Pages 1286-1302

  Goddard, K A B ^a   Yu, C E ^a   Oshima, J ^a   Miki, T ^a   Nakura, J ^a   Piussan, C ^a   Martin, G M ^a   Schellenberg, G D ^a   Wijsman, E M ^a   Brown, W T ^a   Burg, G ^a   Cerimele, D ^a   Cottini, F ^a   Epstein, C J ^a   Fischer, W ^a   Fraccaro, M ^a   Fujiwara, Y ^a   Fukuchi, K I ^a   Hiwada, K ^a  

^a UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 8P; CLINICAL ARTICLE; CONSANGUINEOUS MARRIAGE; CONTROLLED STUDY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCATION; HAPLOTYPE; HUMAN; HUMAN CELL; MUTATION RATE; PEDIGREE; PRIORITY JOURNAL; WERNER SYNDROME;

AGE OF ONSET; ASIAN CONTINENTAL ANCESTRY GROUP; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 8; CONSANGUINITY; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENE FREQUENCY; GENETIC MARKERS; HAPLOTYPES; HUMANS; JAPAN; LINKAGE DISEQUILIBRIUM; MALE; MARKOV CHAINS; MONTE CARLO METHOD; PEDIGREE; WERNER SYNDROME;

EID: 0029971818     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)