Found: 11
Select item for more details and to access through your institution.
A large novel deletion in the APC promoter region causes gene silencing and leads to classical familial adenomatous polyposis in a Manitoba Mennonite kindred.
- Published in:
- Human Genetics, 2008, v. 124, n. 5, p. 535, doi. 10.1007/s00439-008-0579-4
- By:
- Publication type:
- Article
Germline MYH mutations in a clinic-based series of Canadian multiple colorectal adenoma patients.
- Published in:
- Journal of Surgical Oncology, 2007, v. 95, n. 6, p. 499, doi. 10.1002/jso.20724
- By:
- Publication type:
- Article
Psychosocial impact of Peutz-Jeghers Syndrome.
- Published in:
- Familial Cancer, 2009, v. 8, n. 1, p. 59, doi. 10.1007/s10689-008-9202-z
- By:
- Publication type:
- Article
The FAP self-concept scale (adult form).
- Published in:
- Familial Cancer, 2009, v. 8, n. 1, p. 39, doi. 10.1007/s10689-008-9204-x
- By:
- Publication type:
- Article
The history of familial adenomatous polyposis.
- Published in:
- Familial Cancer, 2006, v. 5, n. 3, p. 213, doi. 10.1007/s10689-005-5854-0
- By:
- Publication type:
- Article
Genotype and phenotype of patients with both familial adenomatous polyposis and thyroid carcinoma.
- Published in:
- Familial Cancer, 2003, v. 2, n. 2, p. 95, doi. 10.1023/A:1025762706854
- By:
- Publication type:
- Article
Characterization of two novel adenomatous polyposis coli ( APC) gene mutations in patients with familial adenomatous polyposis (FAP).
- Published in:
- Human Mutation, 1994, v. 4, n. 4, p. 253, doi. 10.1002/humu.1380040404
- By:
- Publication type:
- Article
Juvenile polyposis, hereditary hemorrhagic telangiectasia, and early onset colorectal cancer in patients with SMAD4 mutation.
- Published in:
- Journal of Gastroenterology, 2012, v. 47, n. 7, p. 795, doi. 10.1007/s00535-012-0545-8
- By:
- Publication type:
- Article
A germline mutation at the extreme 3′ end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumor.
- Published in:
- Clinical Genetics, 2000, v. 57, n. 3, p. 205, doi. 10.1034/j.1399-0004.2000.570306.x
- By:
- Publication type:
- Article
STK11/LKB1 germline mutations are not identified in most Peutz–Jeghers syndrome patients.
- Published in:
- Clinical Genetics, 1999, v. 56, n. 2, p. 136, doi. 10.1034/j.1399-0004.1999.560207.x
- By:
- Publication type:
- Article
Identification of somatic APC gene mutations in periampullary adenomas in a patient with familial adenomatous polyposis (FAP).
- Published in:
- Human Molecular Genetics, 1993, v. 2, n. 11, p. 1957
- By:
- Publication type:
- Article