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Volumn 80, Issue 1, 2007, Pages 126-139

Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies

(24)  Pearson, John V a   Huentelman, Matthew J a   Halperin, Rebecca F a   Tembe, Waibhav D a   Melquist, Stacey c   Homer, Nils a   Brun, Marcel a   Szelinger, Szabolcs a   Coon, Keith D a   Zismann, Victoria L a   Webster, Jennifer A a   Beach, Thomas d   Sando, Sigrid B e   Aasly, Jan O f   Heun, Reinhard g   Jessen, Frank g   Kölsch, Heike g   Tsolaki, Magdalini h   Daniilidou, Makrina h   Reiman, Eric M a,b,i   more..


Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ALZHEIMER DISEASE; ARTICLE; CONTROLLED STUDY; COST; DATA ANALYSIS; DATA ANALYSIS SOFTWARE; DISEASE ASSOCIATION; DNA MICROARRAY; EVALUATION; EXPERIMENT; FEMALE; GENE POOL; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC DISORDER; GENETIC PROCEDURES; GENETIC SUSCEPTIBILITY; GENETIC TRAIT; GENOME ANALYSIS; GENOMEWIDE ASSOCIATION; GENOTYPE; GONADAL DYSGENESIS; HERITABILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MATHEMATICAL ANALYSIS; MATHEMATICAL COMPUTING; METHODOLOGY; MICROARRAY ANALYSIS; MOLECULAR PROBE; PRIORITY JOURNAL; PROCESS DEVELOPMENT; PROGRESSIVE SUPRANUCLEAR PALSY; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL MODEL; SUDDEN INFANT DEATH SYNDROME; TECHNIQUE; VALIDATION PROCESS; VALIDATION STUDY;

EID: 33845994780     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/510686     Document Type: Article
Times cited : (136)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.