Origins and functional impact of copy number variation in the human genome

Nature

Volumn 464, Issue 7289, 2010, Pages 704-712

  Conrad, Donald F ^a   Pinto, Dalila ^b   Redon, Richard ^a,c   Feuk, Lars ^b,d   Gokcumen, Omer ^e   Zhang, Yujun ^a   Aerts, Jan ^a   Andrews, T Daniel ^a   Barnes, Chris ^a   Campbell, Peter ^a   Fitzgerald, Tomas ^a   Hu, Min ^a   Ihm, Chun Hwa ^e   Kristiansson, Kati ^a   MacArthur, Daniel G ^a   MacDonald, Jeffrey R ^b   Onyiah, Ifejinelo ^a   Pang, Andy Wing Chun ^b   Robson, Sam ^a   Stirrups, Kathy ^a   Valsesia, Armand ^a   Walter, Klaudia ^a   Wei, John ^b   Tyler Smith, Chris ^a   Carter, Nigel P ^a   Lee, Charles ^e   Scherer, Stephen W ^b,f   Hurles, Matthew E ^a   more..

^a WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c L INSTITUT DU THORAX   (France)

^d UPPSALA UNIVERSITY   (Sweden)

^e HARVARD MEDICAL SCHOOL   (United States)

^f UNIVERSITY OF TORONTO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; GENOME; GENOTYPE; HOMINID;

ARTICLE; DISEASE PREDISPOSITION; DNA MICROARRAY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MUTATION; GENETIC VARIABILITY; GENOTYPE; HERITABILITY; HUMAN GENOME; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

CONTINENTAL POPULATION GROUPS; DNA COPY NUMBER VARIATIONS; GENE DUPLICATION; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HAPLOTYPES; HUMANS; MUTAGENESIS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; REPRODUCIBILITY OF RESULTS;

EID: 77950461601     PISSN: 00280836     EISSN: 14764687     Source Type: Journal    
DOI: 10.1038/nature08516     Document Type: Article

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