Works matching IS 13899600 AND DT 2013 AND VI 12 AND IP 4
Results: 23
The incidence of <i>PALB2</i> c.3113G>A in women with a strong family history of breast and ovarian cancer attending familial cancer centres in Australia.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Whole exome sequencing identifies mutation of EDNRA involved in ACTH-independent macronodular adrenal hyperplasia.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 657, doi. 10.1007/s10689-013-9642-y
- By:
- Publication type:
- Article
Can we test for hereditary cancer at 18 years when we start surveillance at 25? Patient reported outcomes.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 675, doi. 10.1007/s10689-013-9644-9
- By:
- Publication type:
- Article
Rectal cancers in patients with familial adenomatous polyposis.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 749, doi. 10.1007/s10689-013-9656-5
- By:
- Publication type:
- Article
Polymorphisms in arachidonic acid metabolism-related genes and the risk and prognosis of colorectal cancer.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 755, doi. 10.1007/s10689-013-9659-2
- By:
- Publication type:
- Article
Psychosocial consequences of predictive genetic testing for lynch syndrome and associations to surveillance behaviour in a 7-year follow-up study.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 639, doi. 10.1007/s10689-013-9628-9
- By:
- Publication type:
- Article
Novel and recurrent <i>BRCA1/BRCA2</i> mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relationship of family phenotypes with mutation prevalence.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 767, doi. 10.1007/s10689-013-9622-2
- By:
- Publication type:
- Article
Multivariate analysis of <i>MLH1</i> c.1664T>C (p.Leu555Pro) mismatch repair gene variant demonstrates its pathogenicity.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 741, doi. 10.1007/s10689-013-9652-9
- By:
- Publication type:
- Article
Is the psychological impact of genetic testing moderated by support and sharing of test results to family and friends?
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 601, doi. 10.1007/s10689-013-9621-3
- By:
- Publication type:
- Article
Prevalence of <i>HOXB13</i> mutation in a population of Ashkenazi Jewish men treated for prostate cancer.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 597, doi. 10.1007/s10689-013-9618-y
- By:
- Publication type:
- Article
Case report: metachronous central nervous system desmoid tumours and thyroid carcinoma in a young familial adenomatous polyposis patient.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 647, doi. 10.1007/s10689-013-9640-0
- By:
- Publication type:
- Article
The Proceedings of the Collaborative Group of the Americas on Inherited Colorectal Cancer Sheraton Boston Hotel, Boston, Massachusetts, October 27–29, 2012.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 779, doi. 10.1007/s10689-012-9592-9
- Publication type:
- Article
Chemoprevention in Lynch syndrome.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 707, doi. 10.1007/s10689-013-9650-y
- By:
- Publication type:
- Article
Self administered screening for hereditary cancers in conjunction with mammography and ultrasound.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 651, doi. 10.1007/s10689-013-9641-z
- By:
- Publication type:
- Article
Interest of individuals from <i>BRCA</i> families to participate in research studies focused on male <i>BRCA</i> carriers.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 615, doi. 10.1007/s10689-013-9624-0
- By:
- Publication type:
- Article
Do individuals with a family history of colorectal cancer adhere to medical recommendations for the prevention of colorectal cancer?
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 629, doi. 10.1007/s10689-013-9627-x
- By:
- Publication type:
- Article
Factors affecting the decision to undergo risk-reducing salpingo-oophorectomy among women with <i>BRCA</i> gene mutation.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 621, doi. 10.1007/s10689-013-9625-z
- By:
- Publication type:
- Article
Underestimated survival predictions of the prognostic tools Adjuvant! Online and PREDICT in BRCA1-associated breast cancer patients.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 683, doi. 10.1007/s10689-013-9646-7
- By:
- Publication type:
- Article
Extracolonic cancer risk in patients with serrated polyposis syndrome and their first-degree relatives.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 669, doi. 10.1007/s10689-013-9643-x
- By:
- Publication type:
- Article
Association of the BRCA1 promoter polymorphism rs11655505 with the risk of familial breast and/or ovarian cancer.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 691, doi. 10.1007/s10689-013-9647-6
- By:
- Publication type:
- Article
“High rate of recurrent adenomatosis during endoscopic surveillance after duodenectomy in patients with familial adenomatous polyposis”.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 699, doi. 10.1007/s10689-013-9648-5
- By:
- Publication type:
- Article
Phenotypic heterogeneity of hereditary gynecologic cancers: a report from the Creighton hereditary cancer registry.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 719, doi. 10.1007/s10689-013-9651-x
- By:
- Publication type:
- Article
Frameshift mutation in the <i>PTCH2</i> gene can cause nevoid basal cell carcinoma syndrome.
- Published in:
- Familial Cancer, 2013, v. 12, n. 4, p. 611, doi. 10.1007/s10689-013-9623-1
- By:
- Publication type:
- Article