Works matching IS 17312302 AND DT 2015 AND VI 13
Results: 33
Patient experiences living with pancreatic cancer risk.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0034-1
- By:
- Publication type:
- Article
The frequency of BRCA1 founder mutation c.5266dupC (5382insC) in breast cancer patients from Ukraine.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, p. 1, doi. 10.1186/s13053-015-0040-3
- By:
- Publication type:
- Article
Ten modifiers of penetrance BRCA1 validated in a Norwegian series.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0035-0
- By:
- Publication type:
- Article
A case of squamous cell carcinoma of the skin due to the molecularly confirmed Lynch Syndrome.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0033-2
- By:
- Publication type:
- Article
Interest in genomic SNP testing for prostate cancer risk: a pilot survey.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0032-3
- By:
- Publication type:
- Article
The missense variant increases c.470 T > C CHEK2 the risk of differentiated thyroid carcinoma in the Great Poland population.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0030-5
- By:
- Publication type:
- Article
High expression of miR-214 is associated with a worse disease-specific survival of the triple-negative breast cancer patients.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0028-z
- By:
- Publication type:
- Article
High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case report.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0027-0
- By:
- Publication type:
- Article
Molecular diagnosis and comprehensive treatment of multiple endocrine neoplasia type 2 in Southeastern Chinese.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0026-1
- By:
- Publication type:
- Article
Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0025-2
- By:
- Publication type:
- Article
Beliefs about weight and breast cancer: an interview study with high risk women following a 12 month weight loss intervention.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-014-0023-9
- By:
- Publication type:
- Article
Identification of a new large genomic BRCA2 deletion associated with high risk male breast cancer.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-014-0022-x
- By:
- Publication type:
- Article
Next-generation sequencing for genetic testing of familial colorectal cancer syndromes.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, p. 1, doi. 10.1186/s13053-015-0039-9
- By:
- Publication type:
- Article
Next-generation sequencing for genetic testing of familial colorectal cancer syndromes.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0039-9
- By:
- Publication type:
- Article
The role of BRCA1 and BRCA2 mutations in prostate, pancreatic and stomach cancers.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0038-x
- By:
- Publication type:
- Article
Cumulative BRCA mutation analysis in the Greek population confirms that homogenous ethnic background facilitates genetic testing.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0037-y
- By:
- Publication type:
- Article
Tumour spectrum in non-BRCA hereditary breast cancer families in Sweden.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0036-z
- By:
- Publication type:
- Article
Ten modifiers of BRCA1 penetrance validated in a Norwegian series.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0035-0
- By:
- Publication type:
- Article
Patient experiences living with pancreatic cancer risk.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0034-1
- By:
- Publication type:
- Article
A case of squamous cell carcinoma of the skin due to the molecularly confirmed Lynch Syndrome.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0033-2
- By:
- Publication type:
- Article
Interest in genomic SNP testing for prostate cancer risk: a pilot survey.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0032-3
- By:
- Publication type:
- Article
Decisions about prophylactic gynecologic surgery: a qualitative study of the experience of female Lynch syndrome mutation carriers.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0031-4
- By:
- Publication type:
- Article
The c.470 T > C CHEK2 missense variant increases the risk of differentiated thyroid carcinoma in the Great Poland population.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0030-5
- By:
- Publication type:
- Article
Thank you to all our manuscript reviewers in 2014.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0029-y
- By:
- Publication type:
- Article
High expression of miR-214 is associated with a worse disease-specific survival of the triple-negative breast cancer patients.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0028-z
- By:
- Publication type:
- Article
High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case report.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-015-0027-0
- By:
- Publication type:
- Article
Beliefs about weight and breast cancer: an interview study with high risk women following a 12 month weight loss intervention.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-014-0023-9
- By:
- Publication type:
- Article
High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case report.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Molecular diagnosis and comprehensive treatment of multiple endocrine neoplasia type 2 in Southeastern Chinese.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 57, doi. 10.1186/s13053-015-0026-1
- By:
- Publication type:
- Article
PARP inhibitors.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 31, doi. 10.1186/s13053-014-0024-8
- By:
- Publication type:
- Article
Beliefs about weight and breast cancer: an interview study with high risk women following a 12 month weight loss intervention.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 14, doi. 10.1186/s13053-014-0023-9
- By:
- Publication type:
- Article
Identification of a new BRCA2 large genomic deletion associated with high risk male breast cancer.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 1, doi. 10.1186/s13053-014-0022-x
- By:
- Publication type:
- Article
Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families.
- Published in:
- Hereditary Cancer in Clinical Practice, 2015, v. 13, n. 1, p. 39, doi. 10.1186/s13053-015-0025-2
- By:
- Publication type:
- Article