Erratum: Investigation of reported associations between the 20q13 and 21q22 loci and pediatric-onset crohn's disease in canadian children (American Journal of Gastroenterology (2009) DOI:10.1038/ajg.2009.430);Investigation of reported associations between the 20q13 and 21q22 loci and pediatric-onset Crohn's disease in Canadian children

American Journal of Gastroenterology

Volumn 104, Issue 11, 2009, Pages 2824-2828

  Amre, Devendra K ^a,b   Mack, David R ^c   Morgan, Kenneth ^d   Fujiwara, Mary ^d   Israel, David ^e   Deslandres, Colette ^a,b   Seidman, Ernest G ^d   Lambrette, Phlippe ^b   Costea, Irina ^a,b   Krupoves, Alfreda ^a,b   Fegury, Houda ^b   Dong, Jinsong ^b   Grimard, Guy ^a,b   Levy, Emile ^b,f  

^a UNIVERSITÉ DE MONTRÉAL   (Canada)

^b UNIVERSITY OF MONTREAL   (Canada)

^c CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

^d RESEARCH INSTITUTE OF THE MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

^e BC CHILDREN S HOSPITAL   (Canada)

^f UNIVERSITY OF MONTREAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALLELE; ARTICLE; CHROMOSOME 20Q; CHROMOSOME 21; COLON DISEASE; CONTROLLED STUDY; CROHN DISEASE; FEMALE; GENE LOCUS; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; AGE DISTRIBUTION; AGE OF ONSET; CANADA; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 20; CHROMOSOMES, HUMAN, PAIR 21; COHORT STUDIES; CONFIDENCE INTERVALS; CROHN DISEASE; FEMALE; GENE EXPRESSION REGULATION; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; HAPLOTYPES; HUMANS; INCIDENCE; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; REFERENCE VALUES; RISK ASSESSMENT; SEX DISTRIBUTION;

EID: 72049130560     PISSN: 00029270     EISSN: 15720241     Source Type: Journal    
DOI: 10.1038/ajg.2009.527     Document Type: Erratum

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