Long-term outcomes, branch-specific expressivity, and disease-related mortality in von Hippel-Lindau type 2A.
- Published in:
- Familial Cancer, 2011, v. 10, n. 4, p. 701, doi. 10.1007/s10689-011-9465-7
- By:
- Publication type:
- Article
Works matching IS 13899600 AND DT 2011 AND VI 10 AND IP 4
Results: 14
1
2
Concerns about inherited risk of breast cancer prior to diagnosis in Japanese patients with breast complaints.
- Published in:
- Familial Cancer, 2011, v. 10, n. 4, p. 681, doi. 10.1007/s10689-011-9464-8
- By:
- Publication type:
- Article
3
Factors affecting encouragement of relatives among families with Lynch syndrome to seek medical assessment.
- Published in:
- Familial Cancer, 2011, v. 10, n. 4, p. 649, doi. 10.1007/s10689-011-9462-x
- By:
- Publication type:
- Article
4
Limited impact on self-concept in individuals with Lynch syndrome; results from a national cohort study.
- Published in:
- Familial Cancer, 2011, v. 10, n. 4, p. 633, doi. 10.1007/s10689-011-9459-5
- By:
- Publication type:
- Article
5
Abstracts.
- Published in:
- Familial Cancer, 2011, v. 10, n. 4, p. 713, doi. 10.1007/s10689-011-9492-4
- Publication type:
- Article
6
Familial colorectal cancer type X syndrome: two distinct molecular entities?
- Published in:
- Familial Cancer, 2011, v. 10, n. 4, p. 623, doi. 10.1007/s10689-011-9473-7
- By:
- Publication type:
- Article
7
Acinic cell carcinoma of the retromolar trigone region: expanding the tumor phenotype in Cowden syndrome?
- Published in:
- Familial Cancer, 2011, v. 10, n. 4, p. 691, doi. 10.1007/s10689-011-9472-8
- By:
- Publication type:
- Article
8
Microsatellite instability analysis in uterine cavity washings as a screening tool for endometrial cancer in Lynch syndrome.
- Published in:
- Familial Cancer, 2011, v. 10, n. 4, p. 655, doi. 10.1007/s10689-011-9470-x
- By:
- Publication type:
- Article
9
A survey of APC mutations in Quebec.
- Published in:
- Familial Cancer, 2011, v. 10, n. 4, p. 659, doi. 10.1007/s10689-011-9468-4
- By:
- Publication type:
- Article
10
Identification of the deleterious 2080insA BRCA1 mutation in a male renal cell carcinoma patient from a family with multiple cancer diagnoses from Pakistan.
- Published in:
- 2011
- By:
- Publication type:
- Letter
11
Novel nonsense CDC73 mutations in Chinese patients with parathyroid tumors.
- Published in:
- Familial Cancer, 2011, v. 10, n. 4, p. 695, doi. 10.1007/s10689-011-9466-6
- By:
- Publication type:
- Article
12
Communication of BRCA1 and BRCA2 genetic test results to health care providers following genetic testing at a tertiary care center.
- Published in:
- Familial Cancer, 2011, v. 10, n. 4, p. 673, doi. 10.1007/s10689-011-9460-z
- By:
- Publication type:
- Article
13
The identification and management of hereditary diffuse gastric cancer in a large Jordanian family.
- Published in:
- Familial Cancer, 2011, v. 10, n. 4, p. 667, doi. 10.1007/s10689-011-9463-9
- By:
- Publication type:
- Article
14
Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individuals.
- Published in:
- Familial Cancer, 2011, v. 10, n. 4, p. 641, doi. 10.1007/s10689-011-9461-y
- By:
- Publication type:
- Article