Works matching IS 13899600 AND DT 2012 AND VI 11 AND IP 1
Results: 19
Uptake of a randomized breast cancer prevention trial comparing letrozole to placebo in BRCA1/ 2 mutations carriers: the LIBER trial.
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- Familial Cancer, 2012, v. 11, n. 1, p. 77, doi. 10.1007/s10689-011-9484-4
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- Article
The liver: another organ involved in Muir Torre syndrome?
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- Familial Cancer, 2012, v. 11, n. 1, p. 7, doi. 10.1007/s10689-011-9450-1
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- Article
Non-cancer endpoints in BRCA1/2 carriers after risk-reducing salpingo-oophorectomy.
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- Familial Cancer, 2012, v. 11, n. 1, p. 69, doi. 10.1007/s10689-011-9480-8
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- Article
Two novel mutations in hMLH1 gene in Iranian hereditary non-polyposis colorectal cancer patients.
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- Familial Cancer, 2012, v. 11, n. 1, p. 13, doi. 10.1007/s10689-011-9478-2
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- Article
A pre-visit tailored website enhances counselees' realistic expectations and knowledge and fulfils information needs for breast cancer genetic counselling.
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- Familial Cancer, 2012, v. 11, n. 1, p. 85, doi. 10.1007/s10689-011-9479-1
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- Article
BRCA1 and BRCA2 germline mutations in 85 Iranian breast cancer patients.
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- Familial Cancer, 2012, v. 11, n. 1, p. 57, doi. 10.1007/s10689-011-9477-3
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- Article
Case report: a p.C618S RET proto-oncogene germline mutation in a large Chinese pedigree with familial medullary thyroid carcinoma.
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- Familial Cancer, 2012, v. 11, n. 1, p. 131, doi. 10.1007/s10689-011-9487-1
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- Article
Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy.
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- Familial Cancer, 2012, v. 11, n. 1, p. 41, doi. 10.1007/s10689-011-9483-5
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- Article
Implications for cancer genetics practice of pro-actively assessing family history in a General Practice cohort in North West London.
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- Familial Cancer, 2012, v. 11, n. 1, p. 107, doi. 10.1007/s10689-011-9482-6
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- Article
Patient outcomes associated with group and individual genetic counseling formats.
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- Familial Cancer, 2012, v. 11, n. 1, p. 97, doi. 10.1007/s10689-011-9486-2
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- Article
First degree relatives and familial aggregation of gastric cancer: who to choose for control in case-control studies?
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- Familial Cancer, 2012, v. 11, n. 1, p. 137, doi. 10.1007/s10689-011-9488-0
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- Article
Low prevalence of BRCA1 and BRCA2 mutations in the sporadic breast cancer of Spanish population.
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- Familial Cancer, 2012, v. 11, n. 1, p. 49, doi. 10.1007/s10689-011-9481-7
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- Article
Self-reported mammography use following BRCA1/2 genetic testing may be overestimated.
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- Familial Cancer, 2012, v. 11, n. 1, p. 27, doi. 10.1007/s10689-011-9490-6
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- Article
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors.
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- Familial Cancer, 2012, v. 11, n. 1, p. 19, doi. 10.1007/s10689-011-9489-z
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- Article
A state-wide population-based program for detection of lynch syndrome based upon immunohistochemical and molecular testing of colorectal tumours.
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- Familial Cancer, 2012, v. 11, n. 1, p. 1, doi. 10.1007/s10689-011-9494-2
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- Article
Increased incidence of childhood, prostate and breast cancers in relatives of childhood cancer patients.
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- Familial Cancer, 2012, v. 11, n. 1, p. 145, doi. 10.1007/s10689-011-9493-3
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- Article
Evaluation of the BOADICEA risk assessment model in women with a family history of breast cancer.
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- Familial Cancer, 2012, v. 11, n. 1, p. 33, doi. 10.1007/s10689-011-9495-1
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- Article
Familial renal cancer as an indicator of hereditary leiomyomatosis and renal cell cancer syndrome.
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- Familial Cancer, 2012, v. 11, n. 1, p. 115, doi. 10.1007/s10689-011-9485-3
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- Article
Hereditary leiomyomatosis and renal cell cancer presenting as metastatic kidney cancer at 18 years of age: implications for surveillance.
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- Familial Cancer, 2012, v. 11, n. 1, p. 123, doi. 10.1007/s10689-011-9491-5
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- Article