Fine mapping of familial prostate cancer families narrows the interval for a susceptibility locus on chromosome 22q12.3 to 1.36 Mb

Human Genetics

Volumn 123, Issue 1, 2008, Pages 65-75

  Johanneson, Bo ^a   McDonnell, Shannon K ^b   Karyadi, Danielle M ^a   Hebbring, Scott J ^b   Wang, Liang ^b   Deutsch, Kerry ^c   McIntosh, Laura ^d   Kwon, Erika M ^a   Suuriniemi, Miia ^a   Stanford, Janet L ^d,e   Schaid, Daniel J ^b   Ostrander, Elaine A ^a   Thibodeau, Stephen N ^b  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b MAYO CLINIC   (United States)

^c INSTITUTE FOR SYSTEMS BIOLOGY   (United States)

^d Fred Hutchinson Cancer Research Center   (United States)

^e UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 22Q; CHROMOSOME MAP; CONSENSUS SEQUENCE; CONTROLLED STUDY; FAMILIAL CANCER; FAMILY STUDY; GENE LOCUS; GENETIC ASSOCIATION; GENETIC RECOMBINATION; GENETIC SUSCEPTIBILITY; GENOME ANALYSIS; HAPLOTYPE; HIGH RISK POPULATION; HUMAN; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PROSTATE CANCER;

CHROMOSOMES, HUMAN, PAIR 22; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LOD SCORE; MALE; PEDIGREE; PROSTATIC NEOPLASMS;

EID: 38949187963     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-007-0451-y     Document Type: Article

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