Chromosome 8q23.3 and 11q23.1 Variants Modify Colorectal Cancer Risk in Lynch Syndrome

Gastroenterology

Volumn 136, Issue 1, 2009, Pages 131-137

  Wijnen, Juul T ^a   Brohet, Richard M ^b,c   van Eijk, Ronald ^a   Jagmohan Changur, Shanty ^a   Middeldorp, Anneke ^a   Tops, Carli M ^a   van Puijenbroek, Mario ^a   Ausems, Margreet G E M ^d   Gómez García, Encarna ^e   Hes, Frederik J ^a   Hoogerbrugge, Nicoline ^f   Menko, Fred H ^g   van Os, Theo A M ^h   Sijmons, Rolf H ⁱ   Verhoef, Senno ^j   Wagner, Anja ^k   Nagengast, Fokko M ^f   Kleibeuker, Jan H ⁱ   Devilee, Peter ^a   Morreau, Hans ^a   Goldgar, David ^l   Tomlinson, Ian P ^m   Houlston, Richard S ⁿ   van Wezel, Tom ^a   Vasen, Hans F A ^a   more..

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b NETHERLANDS CANCER INSTITUTE   (Netherlands)

^c Infection and Immunology   (Netherlands)

^d UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^e MAASTRICHT UNIVERSITY   (Netherlands)

^f RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^g VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^h ACADEMIC MEDICAL CENTER   (Netherlands)

ⁱ UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^j ANTONI VAN LEEUWENHOEK HOSPITAL   (Netherlands)

^k ERASMUS MEDICAL CENTER   (Netherlands)

^l UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^m IMPERIAL CANCER RESEARCH FUND   (United Kingdom)

ⁿ INSTITUTE OF CANCER RESEARCH   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CANCER RISK; CHROMOSOME VARIANT; COLORECTAL CANCER; CONTROLLED STUDY; FAMILIAL CANCER; FEMALE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; HETEROZYGOTE; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MISMATCH REPAIR; PRIORITY JOURNAL; ADULT; AGED; CHROMOSOME 11; CHROMOSOME 8; COLORECTAL TUMOR; GENETICS; GENOTYPE; MIDDLE AGED; MUTATION; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; AGED; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 8; COLORECTAL NEOPLASMS; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; DNA MISMATCH REPAIR; FEMALE; GENOTYPE; HUMANS; MALE; MIDDLE AGED; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 59849094771     PISSN: 00165085     EISSN: None     Source Type: Journal    
DOI: 10.1053/j.gastro.2008.09.033     Document Type: Article

References (18)

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