Molecular genetic analysis of exons 1 to 6 of the APC gene in non-polyposis familial colorectal cancer
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1995.tb04113.x/fullpdf
Reference36 articles.
1. Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer;Bronner;Nature,1994
2. The UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculations;Burn;J Med Genet,1991
3. Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444;Caspari;Hum Mol Genet,1995
4. Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse;Dietrich;Cell,1993
5. Mutational analysis of the first 14 exons of the adenomatous polyposis coli (APC) gene;Dobbie;Eur J Cancer,1994
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2. Congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial colorectal cancer;Familial Cancer;2006-08-31
3. Genotype phenotype correlations in Israeli colorectal cancer patients;International Journal of Cancer;2005
4. Novel Germline APC Mutations in Swedish Patients with Familial Adenomatous Polyposis and Gardner Syndrome;Scandinavian Journal of Gastroenterology;2000-01
5. APC, MCC;The Oncogene & Tumour Suppressor Gene Factsbook;1997
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