Works matching IS 17312302 AND DT 2017
Results: 22
Meeting abstracts from the Annual Conference on Hereditary Cancers 2016.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0081-x
- Publication type:
- Article
Exome sequencing characterizes the somatic mutation spectrum of early serrated lesions in a patient with serrated polyposis syndrome (SPS).
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0082-9
- By:
- Publication type:
- Article
The BRCA2 variant c.68-7 T>A is associated with breast cancer.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0080-y
- By:
- Publication type:
- Article
Clinical and genetic characterization of hereditary breast cancer in a Chinese population.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0079-4
- By:
- Publication type:
- Article
Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, p. 1, doi. 10.1186/s13053-017-0078-5
- By:
- Publication type:
- Article
Meeting abstracts from the Annual Conference on Hereditary Cancers 2015.
- Published in:
- 2017
- Publication type:
- Abstract
Emotional impact on the results of BRCA1 and BRCA2 genetic test: an observational retrospective study.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0077-6
- By:
- Publication type:
- Article
The potential role of miRNAs in therapy of breast and ovarian cancers associated with BRCA1 mutation.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0076-7
- By:
- Publication type:
- Article
Motivators and barriers of tamoxifen use as risk-reducing medication amongst women at increased breast cancer risk: a systematic literature review.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0075-8
- By:
- Publication type:
- Article
Evaluation of psychosocial aspects in participants of cancer genetic counseling.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0073-x
- By:
- Publication type:
- Article
Hereditary gynaecologic cancers in Nepal: a proposed model of care to serve high risk populations in developing countries.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0072-y
- By:
- Publication type:
- Article
Preoperative genetic testing impacts surgical decision making in BRCA mutation carriers with breast cancer: a retrospective cohort analysis.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0071-z
- By:
- Publication type:
- Article
Late onset asymptomatic pancreatic neuroendocrine tumor -- A case report on the phenotypic expansion for MEN1.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0070-0
- By:
- Publication type:
- Article
Hereditary pancreatic cancer: related syndromes and clinical perspective.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0069-6
- By:
- Publication type:
- Article
ARLTS1 polymorphism is associated with an increased risk of familial cancer: evidence from a meta-analysis.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0068-7
- By:
- Publication type:
- Article
Hereditary and non-hereditary branches of family eligible for BRCA test: cancers in other sites.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0067-8
- By:
- Publication type:
- Article
A case report of Muir-Torre syndrome in a woman with breast cancer and MSI-Low skin squamous cell carcinoma.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
The genetic basis of colonic adenomatous polyposis syndromes.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0065-x
- By:
- Publication type:
- Article
Screening with magnetic resonance imaging, mammography and ultrasound in women at average and intermediate risk of breast cancer.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0064-y
- By:
- Publication type:
- Article
Hereditary cancer syndromes in Latino populations: genetic characterization and surveillance guidelines.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0063-z
- By:
- Publication type:
- Article
Anxiety and depression symptoms among women attending group-based patient education courses for hereditary breast and ovarian cancer.
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-016-0062-5
- By:
- Publication type:
- Article
How does genetic risk information for Lynch syndrome translate to risk management behaviours?
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-016-0061-6
- By:
- Publication type:
- Article