An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1

Journal of Medical Genetics

Volumn 39, Issue 5, 2002, Pages 323-327

  Hutter, Pierre ^a   Wijnen, J ^b   Rey Berthod, C ^a   Thiffault, I ^c   Verkuijlen, P ^b   Farber, D ^c   Hamel, N ^d   Bapat, B ^e   Thibodeau, S N ^f   Burn, J ^g   Wu, J ^h   MacNamara, E ^c   Heinimann, K ⁱ   Chong, G ^c   Foulkes, W D ^c,d,j  

^a Institut Central des Hopitaux Valaisans   (Switzerland)

^b LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^c MCGILL UNIVERSITY   (Canada)

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

^e MOUNT SINAI HOSPITAL   (Canada)

^f MAYO CLINIC   (United States)

^g NEWCASTLE UNIVERSITY   (United Kingdom)

^h ST MARY S HOSPITAL   (United Kingdom)

ⁱ Research Group Human Genetics   (Switzerland)

^j MCGILL UNIVERSITY   (Canada)

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Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUSTRALIA; CANADA; CANCER GENETICS; CASE CONTROL STUDY; COLORECTAL CANCER; CONTROLLED STUDY; DENMARK; DISEASE CARRIER; DNA POLYMORPHISM; GENE; GENE DELETION; GENE MUTATION; GENETIC PREDISPOSITION; GENOTYPE; GERM LINE; GERMANY; HAPLOTYPE; HUMAN; IRELAND; ITALY; MAJOR CLINICAL STUDY; MLH1 GENE; NETHERLANDS; NORWAY; NUCLEIC ACID BASE SUBSTITUTION; PORTUGAL; PRIORITY JOURNAL; SPAIN; SWITZERLAND; TURKEY (REPUBLIC); UNITED KINGDOM; UNITED STATES; YUGOSLAVIA;

EID: 18344393779     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.39.5.323     Document Type: Article

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