Works matching IS 13899600 AND DT 2015 AND VI 14
Results: 80
Birt-Hogg-Dubé syndrome and intracranial vascular pathologies.
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- Familial Cancer, 2015, v. 14, n. 4, p. 595, doi. 10.1007/s10689-015-9807-y
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- 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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- 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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- 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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- 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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- 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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- Article
Supporting families with Cancer: A patient centred survivorship model of care.
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- 2015
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- Publication type:
- Letter
Follicular variant of papillary thyroid cancer in Alström syndrome.
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- Familial Cancer, 2015, v. 14, n. 4, p. 599, doi. 10.1007/s10689-015-9816-x
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- 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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- 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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- 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.
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- Familial Cancer, 2015, v. 14, n. 4, p. 609, doi. 10.1007/s10689-015-9820-1
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- Article
Metastatic sympathetic paraganglioma in a patient with loss of the SDHC gene.
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- Familial Cancer, 2015, v. 14, n. 4, p. 615, doi. 10.1007/s10689-015-9821-0
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- 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.
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- Familial Cancer, 2015, v. 14, n. 4, p. 521, doi. 10.1007/s10689-015-9823-y
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- 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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- Article
Risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: a 30-year semi-prospective analysis.
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- Familial Cancer, 2015, v. 14, n. 4, p. 531, doi. 10.1007/s10689-015-9825-9
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- 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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- Article
Genotype-phenotype analysis of von Hippel-Lindau syndrome in fifteen Indian families.
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- Familial Cancer, 2015, v. 14, n. 4, p. 585, doi. 10.1007/s10689-015-9806-z
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- Publication type:
- Article
Polymorphisms of the XRCC1 gene and breast cancer risk in the Mexican population.
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- Familial Cancer, 2015, v. 14, n. 3, p. 349, doi. 10.1007/s10689-015-9787-y
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- Publication type:
- Article
Timing of risk reducing mastectomy in breast cancer patients carrying a BRCA1/2 mutation: retrospective data from the Dutch HEBON study.
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- Familial Cancer, 2015, v. 14, n. 3, p. 355, doi. 10.1007/s10689-015-9788-x
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- Publication type:
- Article
Heterozygous germline mutations in NBS1 among Korean patients with high-risk breast cancer negative for BRCA1/2 mutation.
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- Familial Cancer, 2015, v. 14, n. 3, p. 365, doi. 10.1007/s10689-015-9789-9
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- Publication type:
- Article
The importance of proper bioinformatics analysis and clinical interpretation of tumor genomic profiling: a case study of undifferentiated sarcoma and a constitutional pathogenic BRCA2 mutation and an MLH1 variant of uncertain significance.
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- Familial Cancer, 2015, v. 14, n. 3, p. 481, doi. 10.1007/s10689-015-9790-3
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- Article
The analysis of a large Danish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 11q24.
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- Familial Cancer, 2015, v. 14, n. 3, p. 393, doi. 10.1007/s10689-015-9791-2
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- Article
Validation of an online questionnaire for identifying people at risk of familial and hereditary colorectal cancer.
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- Familial Cancer, 2015, v. 14, n. 3, p. 401, doi. 10.1007/s10689-015-9792-1
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- Article
Pitfalls in the diagnosis of biallelic PMS2 mutations.
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- Familial Cancer, 2015, v. 14, n. 3, p. 411, doi. 10.1007/s10689-015-9793-0
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- Article
Genetic screening in patients with Retinoblastoma in Israel.
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- Familial Cancer, 2015, v. 14, n. 3, p. 471, doi. 10.1007/s10689-015-9794-z
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- Publication type:
- Article
International society for gastrointestinal hereditary tumours-InSiGHT.
- Published in:
- 2015
- Publication type:
- Abstract
Germline mutations predisposing to non-small cell lung cancer.
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- Familial Cancer, 2015, v. 14, n. 3, p. 463, doi. 10.1007/s10689-015-9796-x
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- Article
Implementing a telephone based peer support intervention for women with a BRCA1/2 mutation.
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- Familial Cancer, 2015, v. 14, n. 3, p. 373, doi. 10.1007/s10689-015-9797-9
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- Article
Risk factors for endometrial cancer among women with a BRCA1 or BRCA2 mutation: a case control study.
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- Familial Cancer, 2015, v. 14, n. 3, p. 383, doi. 10.1007/s10689-015-9798-8
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- Publication type:
- Article
Increased risk for colorectal adenomas and cancer in mono-allelic MUTYH mutation carriers: results from a cohort of North-African Jews.
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- Familial Cancer, 2015, v. 14, n. 3, p. 427, doi. 10.1007/s10689-015-9799-7
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- Article
Clinical characterization and mutation spectrum in Caribbean Hispanic families with Lynch syndrome.
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- Familial Cancer, 2015, v. 14, n. 3, p. 415, doi. 10.1007/s10689-015-9795-y
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- Article
Zebrafish xenotransplantation as a tool for in vivo cancer study.
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- Familial Cancer, 2015, v. 14, n. 3, p. 487, doi. 10.1007/s10689-015-9802-3
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- Article
A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine.
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- Familial Cancer, 2015, v. 14, n. 3, p. 437, doi. 10.1007/s10689-015-9803-2
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- Publication type:
- Article
3′-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivity.
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- Familial Cancer, 2015, v. 14, n. 3, p. 449, doi. 10.1007/s10689-015-9804-1
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- Article
Analysis of PALB2 in a cohort of Italian breast cancer patients: identification of a novel PALB2 truncating mutation.
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- 2015
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- Publication type:
- Letter
Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz-Jeghers syndrome.
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- Familial Cancer, 2015, v. 14, n. 3, p. 455, doi. 10.1007/s10689-015-9800-5
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- Article
Health professionals' evaluation of delivering treatment-focused genetic testing to women newly diagnosed with breast cancer.
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- Familial Cancer, 2015, v. 14, n. 2, p. 265, doi. 10.1007/s10689-014-9770-z
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- Publication type:
- Article
First-Line sunitinib in patients with renal cell carcinoma (RCC) in von Hippel-Lindau (VHL) disease: clinical outcome and patterns of radiological response.
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- Familial Cancer, 2015, v. 14, n. 2, p. 309, doi. 10.1007/s10689-014-9771-y
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- Publication type:
- Article
Desmoid tumors: clinical features and outcome of an unpredictable and challenging manifestation of familial adenomatous polyposis.
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- Familial Cancer, 2015, v. 14, n. 2, p. 211, doi. 10.1007/s10689-014-9772-x
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- Publication type:
- Article
Comparison of proctocolectomy and ileal pouch-anal anastomosis to colectomy and ileorectal anastomosis in familial adenomatous polyposis.
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- Familial Cancer, 2015, v. 14, n. 2, p. 221, doi. 10.1007/s10689-014-9773-9
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- Publication type:
- Article
Parental age and Neurofibromatosis Type 1: a report from the NF1 Patient Registry Initiative.
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- Familial Cancer, 2015, v. 14, n. 2, p. 317, doi. 10.1007/s10689-014-9774-8
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- Article
The roles of AXIN2 in tumorigenesis and epigenetic regulation.
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- Familial Cancer, 2015, v. 14, n. 2, p. 325, doi. 10.1007/s10689-014-9775-7
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- Publication type:
- Article
A risk of digestive tract neoplasms susceptibility in miR-146a and miR-196a2.
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- Familial Cancer, 2015, v. 14, n. 2, p. 229, doi. 10.1007/s10689-014-9776-6
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- Publication type:
- Article
Impact of BRCA1/ 2 mutation on young women's 5-year parenthood rates: a prospective comparative study (GENEPSO-PS cohort).
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- Familial Cancer, 2015, v. 14, n. 2, p. 273, doi. 10.1007/s10689-014-9777-5
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- Publication type:
- Article
Exome sequencing reveals three novel candidate predisposition genes for diffuse gastric cancer.
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- Familial Cancer, 2015, v. 14, n. 2, p. 241, doi. 10.1007/s10689-015-9778-z
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- Publication type:
- Article
The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriers.
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- Familial Cancer, 2015, v. 14, n. 2, p. 333, doi. 10.1007/s10689-015-9779-y
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- Publication type:
- Article