A comprehensive analysis of common copy-number variations in the human genome

American Journal of Human Genetics

Volumn 80, Issue 1, 2007, Pages 91-104

  Wong, Kendy K ^a,c   DeLeeuw, Ronald J ^a   Dosanjh, Nirpjit S ^a   Kimm, Lindsey R ^a   Cheng, Ze ^b   Horsman, Douglas E ^a   MacAulay, Calum ^a   Ng, Raymond T ^a   Brown, Carolyn J ^a   Eichler, Evan E ^b   Lam, Wan L ^a  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

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

^c NONE   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

MICRORNA;

ARTICLE; AUTOSOME; BLOOD GROUP RHESUS SYSTEM; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; COPY NUMBER VARIATION; DEVELOPMENTAL DISORDER; DISEASE PREDISPOSITION; FEMALE; GENE FREQUENCY; GENE IDENTIFICATION; GENE LOCATION; GENE LOCUS; GENE NUMBER; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOME ANALYSIS; GENOME SIZE; GENOTYPE PHENOTYPE CORRELATION; HEARING; HUMAN; HUMAN GENOME; MAJOR CLINICAL STUDY; MALE; METABOLISM; PHENOTYPIC VARIATION; POLYMORPHIC LOCUS; POPULATION GENETICS; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SMELLING; TASTE; VISION;

EID: 33846006596     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/510560     Document Type: Article

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