Works matching IS 17312302 AND DT 2014 AND VI 12 AND IP 1
Results: 17
Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-20
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- Publication type:
- Article
Germline MUTYH gene mutations are not frequently found in unselected patients with papillary breast carcinoma.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-21
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- Publication type:
- Article
Large deletion causing von Hippel-Lindau disease and hereditary breast cancer syndrome.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-16
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- Publication type:
- Article
Expanding the genetic basis of copy number variation in familial breast cancer.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-15
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- Publication type:
- Article
Familial cancer among consecutive uterine cancer patients in Sweden.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-14
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- Publication type:
- Article
The role of Wnt signaling pathway in carcinogenesis and implications for anticancer therapeutics.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-13
- By:
- Publication type:
- Article
The Norwegian PMS2 founder mutation c.989-1G > T shows high penetrance of microsatellite instable cancers with normal immunohistochemistry.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-12
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- Publication type:
- Article
TP53 p.R337H prevalence in a series of Brazilian hereditary breast cancer families.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-8
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- Publication type:
- Article
Prevalence of BRCA1 and BRCA2 mutations in unselected breast cancer patients from medellín, Colombia.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-11
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- Publication type:
- Article
Colorectal cancer and self-reported tooth agenesis.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-7
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- Publication type:
- Article
A risk of breast cancer in women - carriers of constitutional CHEK2 gene mutations, originating from the North - Central Poland.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-10
- By:
- Publication type:
- Article
Dupuytren's disease and the risk of malignant neoplasms.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-6
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- Publication type:
- Article
Neurofibromatosis type I with breast cancer: not only for women!
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-5
- By:
- Publication type:
- Article
Gastric adenomas in familial adenomatous polyposis are common, but subtle, and have a benign course.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-4
- By:
- Publication type:
- Article
Familial testicular germ cell tumor: no associated syndromic pattern identified.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-3
- By:
- Publication type:
- Article
Plasma homocysteine levels and genetic polymorphisms in folate metablism are associated with breast cancer risk in chinese women.
- Published in:
- Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-2
- By:
- Publication type:
- Article
Patient-reported disease knowledge and educational needs in Lynch syndrome: findings of an interactive multidisciplinary patient conference.
- Published in:
- 2014
- By:
- Publication type:
- Proceeding