Works matching IS 13899600 AND DT 2018 AND VI 17 AND IP 3
Results: 20
Information and support needs of young women regarding breast cancer risk and genetic testing: adapting effective interventions for a novel population.
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- Familial Cancer, 2018, v. 17, n. 3, p. 351, doi. 10.1007/s10689-017-0059-x
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Genotype phenotype correlation in Asian Indian von Hippel-Lindau (VHL) syndrome patients with pheochromocytoma/paraganglioma.
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- Familial Cancer, 2018, v. 17, n. 3, p. 441, doi. 10.1007/s10689-017-0058-y
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Association between miR-146a rs2910164 polymorphism and specific cancer susceptibility: an updated meta-analysis.
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- Familial Cancer, 2018, v. 17, n. 3, p. 459, doi. 10.1007/s10689-017-0056-0
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Excluding Lynch syndrome in a female patient with metachronous DNA mismatch repair deficient colon- and ovarian cancer.
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- Familial Cancer, 2018, v. 17, n. 3, p. 415, doi. 10.1007/s10689-017-0055-1
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Germline variant in MSX1 identified in a Dutch family with clustering of Barrett’s esophagus and esophageal adenocarcinoma.
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- Familial Cancer, 2018, v. 17, n. 3, p. 435, doi. 10.1007/s10689-017-0054-2
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- Article
Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge.
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- Familial Cancer, 2018, v. 17, n. 3, p. 403, doi. 10.1007/s10689-017-0053-3
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Universal determination of microsatellite instability using BAT26 as a single marker in an Argentine colorectal cancer cohort.
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- Familial Cancer, 2018, v. 17, n. 3, p. 395, doi. 10.1007/s10689-017-0052-4
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- Article
Family history influences the tumor characteristics and prognosis of breast cancers developing during postmenopausal hormone therapy.
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- Familial Cancer, 2018, v. 17, n. 3, p. 321, doi. 10.1007/s10689-017-0046-2
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Targeted massively parallel sequencing characterises the mutation spectrum of PALB2 in breast and ovarian cancer cases from Poland and Ukraine.
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- Familial Cancer, 2018, v. 17, n. 3, p. 345, doi. 10.1007/s10689-017-0050-6
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- Article
Cost-effectiveness evaluation of pre-counseling telephone interviews before face-to-face genetic counseling in cancer genetics.
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- Familial Cancer, 2018, v. 17, n. 3, p. 451, doi. 10.1007/s10689-017-0049-z
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Penetrance of a rare familial mutation predisposing to papillary thyroid cancer.
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- Familial Cancer, 2018, v. 17, n. 3, p. 431, doi. 10.1007/s10689-017-0048-0
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Cancer risk management in Tasmanian women with BRCA1 and BRCA2 mutations.
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- Familial Cancer, 2018, v. 17, n. 3, p. 333, doi. 10.1007/s10689-017-0047-1
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Corrections to: Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries.
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- Familial Cancer, 2018, v. 17, n. 3, p. 469, doi. 10.1007/s10689-017-0051-5
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- Article
Germline mutations in lung cancer and personalized medicine.
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- Familial Cancer, 2018, v. 17, n. 3, p. 429, doi. 10.1007/s10689-017-0044-4
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Screening for germline mutations in mismatch repair genes in patients with Lynch syndrome by next generation sequencing.
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- Familial Cancer, 2018, v. 17, n. 3, p. 387, doi. 10.1007/s10689-017-0043-5
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Ectopic, retroperitoneal adrenocortical carcinoma in the setting of Lynch syndrome.
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- Familial Cancer, 2018, v. 17, n. 3, p. 381, doi. 10.1007/s10689-017-0042-6
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- Article
Evaluation of an online family history tool for identifying hereditary and familial colorectal cancer.
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- Familial Cancer, 2018, v. 17, n. 3, p. 371, doi. 10.1007/s10689-017-0041-7
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- Article
Evaluation of current prediction models for Lynch syndrome: updating the PREMM5 model to identify PMS2 mutation carriers.
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- Familial Cancer, 2018, v. 17, n. 3, p. 361, doi. 10.1007/s10689-017-0039-1
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- Article
An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review.
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- Familial Cancer, 2018, v. 17, n. 3, p. 421, doi. 10.1007/s10689-017-0037-3
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- Article
Increased access to TP53 analysis through breast cancer multi-gene panels: clinical considerations.
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- Familial Cancer, 2018, v. 17, n. 3, p. 317, doi. 10.1007/s10689-017-0020-z
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