Works matching IS 13899600 AND DT 2015 AND VI 14 AND IP 4
Results: 21
Birt-Hogg-Dubé syndrome and intracranial vascular pathologies.
- Published in:
- Familial Cancer, 2015, v. 14, n. 4, p. 595, doi. 10.1007/s10689-015-9807-y
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- Publication type:
- Article
Prevalence and detection of psychosocial problems in cancer genetic counseling.
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- Familial Cancer, 2015, v. 14, n. 4, p. 629, doi. 10.1007/s10689-015-9809-9
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- Publication type:
- Article
Childhood cancers in families with and without Lynch syndrome.
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- Familial Cancer, 2015, v. 14, n. 4, p. 545, doi. 10.1007/s10689-015-9810-3
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- Article
Psychological distress related to BRCA testing in ovarian cancer patients.
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- Familial Cancer, 2015, v. 14, n. 4, p. 495, doi. 10.1007/s10689-015-9811-2
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- Publication type:
- Article
Survival in familial colorectal cancer: a Danish cohort study.
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- Familial Cancer, 2015, v. 14, n. 4, p. 553, doi. 10.1007/s10689-015-9812-1
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- Publication type:
- Article
Challenges to clinical utilization of hereditary cancer gene panel testing: perspectives from the front lines.
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- Familial Cancer, 2015, v. 14, n. 4, p. 641, doi. 10.1007/s10689-015-9817-9
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- Publication type:
- Article
Coexistence of paraganglioma/pheochromocytoma and papillary thyroid carcinoma: a four-case series analysis.
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- Familial Cancer, 2015, v. 14, n. 4, p. 603, doi. 10.1007/s10689-015-9818-8
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- Publication type:
- Article
Supporting families with Cancer: A patient centred survivorship model of care.
- Published in:
- 2015
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- Publication type:
- Letter
Follicular variant of papillary thyroid cancer in Alström syndrome.
- Published in:
- Familial Cancer, 2015, v. 14, n. 4, p. 599, doi. 10.1007/s10689-015-9816-x
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- Publication type:
- Article
A functional HOTAIR rs920778 polymorphism does not contributes to gastric cancer in a Turkish population: a case-control study.
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- Familial Cancer, 2015, v. 14, n. 4, p. 561, doi. 10.1007/s10689-015-9813-0
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- Publication type:
- Article
BRCA1 gene variant p.P142H associated with male breast cancer: a two-generation genealogic study and literature review.
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- Familial Cancer, 2015, v. 14, n. 4, p. 515, doi. 10.1007/s10689-015-9819-7
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- Publication type:
- Article
BRCA1 and BRCA2 mutations in males with familial breast and ovarian cancer syndrome. Results of a Spanish multicenter study.
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- Familial Cancer, 2015, v. 14, n. 4, p. 505, doi. 10.1007/s10689-015-9814-z
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- Publication type:
- Article
High accuracy of family history of melanoma in Danish melanoma cases.
- Published in:
- Familial Cancer, 2015, v. 14, n. 4, p. 609, doi. 10.1007/s10689-015-9820-1
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- Publication type:
- Article
Metastatic sympathetic paraganglioma in a patient with loss of the SDHC gene.
- Published in:
- Familial Cancer, 2015, v. 14, n. 4, p. 615, doi. 10.1007/s10689-015-9821-0
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- Publication type:
- Article
Massive gastric polyposis associated with a germline SMAD4 gene mutation.
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- Familial Cancer, 2015, v. 14, n. 4, p. 569, doi. 10.1007/s10689-015-9822-z
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- Publication type:
- Article
Risk reducing salpingectomy and delayed oophorectomy in high risk women: views of cancer geneticists, genetic counsellors and gynaecological oncologists in the UK.
- Published in:
- Familial Cancer, 2015, v. 14, n. 4, p. 521, doi. 10.1007/s10689-015-9823-y
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- Publication type:
- Article
Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene.
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- Familial Cancer, 2015, v. 14, n. 4, p. 575, doi. 10.1007/s10689-015-9824-x
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- Publication type:
- Article
Risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: a 30-year semi-prospective analysis.
- Published in:
- Familial Cancer, 2015, v. 14, n. 4, p. 531, doi. 10.1007/s10689-015-9825-9
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- Publication type:
- Article
POLE mutations in families predisposed to cutaneous melanoma.
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- Familial Cancer, 2015, v. 14, n. 4, p. 621, doi. 10.1007/s10689-015-9826-8
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- Publication type:
- Article
The effect of personal medical history and family history of cancer on the uptake of risk-reducing salpingo-oophorectomy.
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- Familial Cancer, 2015, v. 14, n. 4, p. 539, doi. 10.1007/s10689-015-9827-7
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- Publication type:
- Article
Genotype-phenotype analysis of von Hippel-Lindau syndrome in fifteen Indian families.
- Published in:
- Familial Cancer, 2015, v. 14, n. 4, p. 585, doi. 10.1007/s10689-015-9806-z
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- Publication type:
- Article