Found: 25
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Online decision support for persons having a genetic predisposition to cancer and their partners during reproductive decision‐making.
- Published in:
- Journal of Genetic Counseling, 2019, v. 28, n. 3, p. 533, doi. 10.1002/jgc4.1056
- By:
- Publication type:
- Article
An E-Learning Module to Improve Nongenetic Health Professionals' Assessment of Colorectal Cancer Genetic Risk: Feasibility Study.
- Published in:
- Journal of Medical Internet Research, 2017, v. 19, n. 12, p. 1, doi. 10.2196/mededu.7173
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- Publication type:
- Article
Routine testing for PALB2 mutations in familial pancreatic cancer families and breast cancer families with pancreatic cancer is not indicated.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 5, p. 577, doi. 10.1038/ejhg.2011.226
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- Publication type:
- Article
ASO Visual Abstract: Surgical Oncologists and Nurses in Breast Cancer Care are Ready to Provide Pre-Test Genetic Counseling.
- Published in:
- 2023
- By:
- Publication type:
- Abstract
Addition of an online, validated family history questionnaire to the Dutch FIT-based screening programme did not improve its diagnostic yield.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS): a prospective, observational, multi-center study.
- Published in:
- Familial Cancer, 2021, v. 20, n. 4, p. 263, doi. 10.1007/s10689-021-00237-1
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- Publication type:
- Article
'We don't know for sure': discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations.
- Published in:
- Familial Cancer, 2020, v. 19, n. 1, p. 65, doi. 10.1007/s10689-019-00154-4
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- Publication type:
- Article
The development of an online decision aid to support persons having a genetic predisposition to cancer and their partners during reproductive decision-making: a usability and pilot study.
- Published in:
- Familial Cancer, 2019, v. 18, n. 1, p. 137, doi. 10.1007/s10689-018-0092-4
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- Publication type:
- Article
A scoping review of practice recommendations for clinicians' communication of uncertainty.
- Published in:
- Health Expectations, 2021, v. 24, n. 4, p. 1025, doi. 10.1111/hex.13255
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- Publication type:
- Article
Informing relatives about their hereditary or familial cancer risk: study protocol for a randomized controlled trial.
- Published in:
- Trials, 2014, v. 15, n. 1, p. 86, doi. 10.1186/1745-6215-15-86
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- Publication type:
- Article
Informing relatives about their hereditary or familial cancer risk: study protocol for a randomized controlled trial.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Germline CDKN1B/p27<sup>Kip1</sup> Mutation in Multiple Endocrine Neoplasia.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 8, p. 3321, doi. 10.1210/jc.2006-2843
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- Publication type:
- Article
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer.
- Published in:
- NPJ Breast Cancer, 2019, v. 5, n. 1, p. N.PAG, doi. 10.1038/s41523-019-0127-5
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- Publication type:
- Article
Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case-control study.
- Published in:
- BMC Research Notes, 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13104-015-1235-4
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- Publication type:
- Article
A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: Determination of the molecular basis.
- Published in:
- Human Mutation, 2000, v. 16, n. 1, p. 18, doi. 10.1002/1098-1004(200007)16:1<18::AID-HUMU4>3.0.CO;2-N
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- Publication type:
- Article
Asn540Thr substitution in the fibroblast growth factor receptor 3 tyrosine kinase domain causing hypochondroplasia.
- Published in:
- Human Mutation, 1998, v. 11, p. S62, doi. 10.1002/humu.1380110122
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- Publication type:
- Article
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification.
- Published in:
- Human Mutation, 2019, v. 40, n. 9, p. 1557, doi. 10.1002/humu.23818
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- Publication type:
- Article
Referral for genetic counselling during pregnancy: limited alertness and awareness about genetic risk factors among GPs.
- Published in:
- 2003
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- Publication type:
- journal article
Two supernumerary marker chromosomes, derived from chromosome 6 and 9, in a boy with mild developmental delay.
- Published in:
- Clinical Genetics, 1996, v. 49, n. 1, p. 42, doi. 10.1111/j.1399-0004.1996.tb04323.x
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- Publication type:
- Article
Repeated participation in pancreatic cancer surveillance by high-risk individuals imposes low psychological burden.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 9, p. 1769, doi. 10.1093/hmg/8.9.1769
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- Publication type:
- Article
Improved overall survival after contralateral risk-reducing mastectomy in BRCA1/2 mutation carriers with a history of unilateral breast cancer: A prospective analysis.
- Published in:
- International Journal of Cancer, 2015, v. 136, n. 3, p. 668, doi. 10.1002/ijc.29032
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- Publication type:
- Article
Relevance and efficacy of breast cancer screening in BRCA1 and BRCA2 mutation carriers above 60 years: A national cohort study.
- Published in:
- International Journal of Cancer, 2014, v. 135, n. 12, p. 2940, doi. 10.1002/ijc.28941
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- Publication type:
- Article
Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers.
- Published in:
- 2019
- By:
- Publication type:
- journal article