Found: 20
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Letter to the editor.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 565, doi. 10.1007/s10689-018-0069-3
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- Publication type:
- Article
Adaptation of couples living with a high risk of breast/ovarian cancer and the association with risk-reducing surgery.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 485, doi. 10.1007/s10689-017-0065-z
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- Publication type:
- Article
Molecular analysis of an asbestos-exposed Belgian family with a high prevalence of mesothelioma.
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- Familial Cancer, 2018, v. 17, n. 4, p. 569, doi. 10.1007/s10689-018-0095-1
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- Article
Discussions about predictive genetic testing for Lynch syndrome: the role of health professionals and families in decisions to decline.
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- Familial Cancer, 2018, v. 17, n. 4, p. 547, doi. 10.1007/s10689-018-0078-2
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- Publication type:
- Article
Response to letter to editor regarding published article—metachronous colorectal cancer following segmental or extended colectomy in Lynch syndrome: a systematic review and meta-analysis.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 545, doi. 10.1007/s10689-018-0077-3
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- Publication type:
- Article
A retrospective review of 48 individuals, including 12 families, molecularly diagnosed with hereditary leiomyomatosis and renal cell cancer (HLRCC).
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 615, doi. 10.1007/s10689-018-0076-4
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- Publication type:
- Article
The first two confirmed sub-Saharan African families with germline TP53 mutations causing Li-Fraumeni syndrome.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 607, doi. 10.1007/s10689-018-0075-5
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- Publication type:
- Article
Commentary: PREMM5 threshold of 2.5% is recommended to improve identification of PMS2 carriers.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 567, doi. 10.1007/s10689-018-0074-6
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- Publication type:
- Article
Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 601, doi. 10.1007/s10689-018-0073-7
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- Publication type:
- Article
APC mosaicism in a young woman with desmoid type fibromatosis and familial adenomatous polyposis.
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- Familial Cancer, 2018, v. 17, n. 4, p. 539, doi. 10.1007/s10689-018-0072-8
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- Publication type:
- Article
Risk management adherence following genetic testing for hereditary cancer syndromes: a Singaporean experience.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 621, doi. 10.1007/s10689-018-0071-9
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- Publication type:
- Article
Clinical interpretation of pathogenic ATM and CHEK2 variants on multigene panel tests: navigating moderate risk.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 495, doi. 10.1007/s10689-018-0070-x
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- Publication type:
- Article
Gene expression analysis in peripheral blood cells of patients with hereditary leiomyomatosis and renal cell cancer syndrome (HLRCC): identification of NRF2 pathway activation.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 587, doi. 10.1007/s10689-017-0068-9
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- Publication type:
- Article
Haplotype analysis suggest that the MLH1 c.2059C > T mutation is a Swedish founder mutation.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 531, doi. 10.1007/s10689-017-0067-x
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- Publication type:
- Article
Feasibility of endoscopic resection using bipolar snare for nonampullary duodenal tumours in familial adenomatous polyposis patients.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 517, doi. 10.1007/s10689-017-0063-1
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- Publication type:
- Article
Urological sequelae of desmoids associated with familial adenomatous polyposis.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 525, doi. 10.1007/s10689-017-0064-0
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- Publication type:
- Article
Metachronous colorectal cancer following segmental or extended colectomy in Lynch syndrome: a systematic review and meta-analysis.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 557, doi. 10.1007/s10689-017-0062-2
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- Publication type:
- Article
SNP association study in PMS2-associated Lynch syndrome.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 507, doi. 10.1007/s10689-017-0061-3
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- Publication type:
- Article
Correlation of IL-31 gene polymorphisms with susceptibility and clinical recurrence of bladder cancer.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 577, doi. 10.1007/s10689-017-0060-4
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- Publication type:
- Article
Mutations in context: implications of BRCA testing in diverse populations.
- Published in:
- Familial Cancer, 2018, v. 17, n. 4, p. 471, doi. 10.1007/s10689-017-0038-2
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- Publication type:
- Article