Works matching IS 17312302 AND DT 2013 AND VI 11 AND IP 1
Results: 15
Hereditary cancer risk assessment: essential tools for a better approach.
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- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 39, doi. 10.1186/1897-4287-11-16
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- Publication type:
- Article
Familial adenomatous polyposis of the colon.
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- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 21, doi. 10.1186/1897-4287-11-15
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- Publication type:
- Article
Experience of BRCA1/2 mutation-negative young women from families with hereditary breast and ovarian cancer: a qualitative study.
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- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-14
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- Publication type:
- Article
Hereditary breast cancer: ever more pieces to the polygenic puzzle.
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- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-12
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- Publication type:
- Article
Acute myeloid leukemia in a 38-year-old hemodialyzed patient with von Hippel-Lindau disease.
- Published in:
- 2013
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- Publication type:
- Case Study
Germline deletions in the EPCAM gene as a cause of Lynch syndrome - literature review.
- Published in:
- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-9
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- Publication type:
- Article
Differential expression of PTEN gene correlates with phenotypic heterogeneity in three cases of patients showing clinical manifestations of PTEN hamartoma tumour syndrome.
- Published in:
- 2013
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- Publication type:
- Case Study
Comparison of whole genome amplification and nested-PCR methods for preimplantation genetic diagnosis for BRCA1 gene mutation on unfertilized oocytes-a pilot study.
- Published in:
- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-10
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- Publication type:
- Article
Sense of coherence and self-concept in Lynch syndrome.
- Published in:
- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-7
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- Publication type:
- Article
Psoriasis vulgaris and familial cancer riska population-based study.
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- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-6
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- Publication type:
- Article
Carcinogenesis of PIK3CA.
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- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-5
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- Publication type:
- Article
The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients.
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- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-20
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- Publication type:
- Article
The impact of genetic variants in inflammatory-related genes on prostate cancer risk among men of African Descent: a case control study.
- Published in:
- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-19
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- Publication type:
- Article
Mutation spectrum in South American Lynch syndrome families.
- Published in:
- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-18
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- Publication type:
- Article
Optimizing recruitment to a prostate cancer surveillance program among male BRCA1 mutation carriers: invitation by mail or by telephone.
- Published in:
- Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-17
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- Publication type:
- Article