Is there an association between invasive lobular carcinoma of the breast and a family history of gastric cancer?
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 41, doi. 10.1007/s10689-015-9833-9
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- Publication type:
- Article
Works matching IS 13899600 AND DT 2016 AND VI 15 AND IP 1
Results: 18
1
2
Long-term outcome of sporadic and FAP-associated desmoid tumors treated with high-dose selective estrogen receptor modulators and sulindac: a single-center long-term observational study in 134 patients.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 31, doi. 10.1007/s10689-015-9830-z
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- Publication type:
- Article
3
The role of germline mutations in the BRCA1/2 and mismatch repair genes in men ascertained for early-onset and/or familial prostate cancer.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 111, doi. 10.1007/s10689-015-9832-x
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- Publication type:
- Article
4
Incidental diagnosis of HLRCC following investigation for Asperger Syndrome: actionable and actioned.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 25, doi. 10.1007/s10689-015-9829-5
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- Publication type:
- Article
5
Ovarian tumors related to intronic mutations in DICER1: a report from the international ovarian and testicular stromal tumor registry.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 105, doi. 10.1007/s10689-015-9831-y
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- Publication type:
- Article
6
Screening of HELQ in breast and ovarian cancer families.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 19, doi. 10.1007/s10689-015-9838-4
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- Publication type:
- Article
7
Aortopulmonary window parathyroid gland causing primary hyperparathyroidism in men type 1 syndrome.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 133, doi. 10.1007/s10689-015-9840-x
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- Publication type:
- Article
8
Association of APC I1307K and E1317Q polymorphisms with colorectal cancer among Egyptian subjects.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 49, doi. 10.1007/s10689-015-9834-8
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- Publication type:
- Article
9
The knowledge value-chain of genetic counseling for breast cancer: an empirical assessment of prediction and communication processes.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 1, doi. 10.1007/s10689-015-9835-7
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- Publication type:
- Article
10
Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicism.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 123, doi. 10.1007/s10689-015-9836-6
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- Publication type:
- Article
11
Birt-Hogg-Dubé syndrome: novel FLCN frameshift deletion in daughter and father with renal cell carcinomas.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 127, doi. 10.1007/s10689-015-9837-5
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- Publication type:
- Article
12
Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 85, doi. 10.1007/s10689-015-9845-5
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- Publication type:
- Article
13
First report of somatic mosaicism for mutations in STK11 in four patients with Peutz-Jeghers syndrome.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 57, doi. 10.1007/s10689-015-9839-3
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- Publication type:
- Article
14
Germline TERT promoter mutations are rare in familial melanoma.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 139, doi. 10.1007/s10689-015-9841-9
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- Publication type:
- Article
15
Genetic testing for Lynch syndrome: family communication and motivation.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 63, doi. 10.1007/s10689-015-9842-8
- By:
- Publication type:
- Article
16
Association between the FTOrs8050136 polymorphism and cancer risk: a meta-analysis.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 145, doi. 10.1007/s10689-015-9843-7
- By:
- Publication type:
- Article
17
Surveillance using capsule endoscopy is safe in post-colectomy patients with familial adenomatous polyposis: a prospective Japanese study.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 75, doi. 10.1007/s10689-015-9844-6
- By:
- Publication type:
- Article
18
Screening of RET gene mutations in Chinese patients with medullary thyroid carcinoma and their relatives.
- Published in:
- Familial Cancer, 2016, v. 15, n. 1, p. 99, doi. 10.1007/s10689-015-9828-6
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- Publication type:
- Article