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Results: 4

1.

CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure.

Vermeire S, Wild G, Kocher K, Cousineau J, Dufresne L, Bitton A, Langelier D, Pare P, Lapointe G, Cohen A, Daly MJ, Rioux JD.

Am J Hum Genet. 2002 Jul;71(1):74-83. Epub 2002 May 17.

PMID:
12019468
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

CARD15 mutations in Dutch familial and sporadic inflammatory bowel disease and an overview of European studies.

van der Linde K, Boor PP, Houwing-Duistermaat JJ, Crusius BJ, Wilson PJ, Kuipers EJ, de Rooij FW.

Eur J Gastroenterol Hepatol. 2007 Jun;19(6):449-59. Review.

PMID:
17489054
[PubMed - indexed for MEDLINE]
3.

Alterations of the CARD15/NOD2 gene and the impact on management and treatment of Crohn's disease patients.

Török HP, Glas J, Lohse P, Folwaczny C.

Dig Dis. 2003;21(4):339-45. Review.

PMID:
14752224
[PubMed - indexed for MEDLINE]
4.

Sequence variation at the human ABO locus.

Yip SP.

Ann Hum Genet. 2002 Jan;66(Pt 1):1-27. Review.

PMID:
12014997
[PubMed - indexed for MEDLINE]

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