Found: 18
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Uniparental disomy with and without confined placental mosaicism: a model for trisomic zygote rescue.
- Published in:
- Prenatal Diagnosis, 1998, v. 18, n. 7, p. 659, doi. 10.1002/(SICI)1097-0223(199807)18:7<659::AID-PD317>3.0.CO;2-K
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- Article
Recurrent HOXB13 mutations in the Dutch population do not associate with increased breast cancer risk.
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- Scientific Reports, 2016, p. 30026, doi. 10.1038/srep30026
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- Article
Psychological distress and use of psychosocial support in familial adenomatous polyposis.
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- Psycho-Oncology, 2010, v. 19, n. 3, p. 289, doi. 10.1002/pon.1570
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- Article
Evaluation of the Dutch BRCA1/2 clinical genetic center referral criteria in an unselected early breast cancer population.
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- European Journal of Human Genetics, 2015, v. 23, n. 5, p. 588, doi. 10.1038/ejhg.2014.161
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- Article
Attitudes toward genetic testing in childhood and reproductive decision-making for familial adenomatous polyposis.
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- European Journal of Human Genetics, 2010, v. 18, n. 2, p. 186, doi. 10.1038/ejhg.2009.151
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- Article
The single-nucleotide polymorphism 309 in the MDM2 gene contributes to the Li–Fraumeni syndrome and related phenotypes.
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- European Journal of Human Genetics, 2007, v. 15, n. 1, p. 110, doi. 10.1038/sj.ejhg.5201715
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- Article
Mutational analysis of the TSC1 and TSC2 genes in a diagnostic setting: genotype-phenotype correlations and comparison of diagnostic DNA techniques in Tuberous Sclerosis Complex.
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- European Journal of Human Genetics, 2005, v. 13, n. 6, p. 731, doi. 10.1038/sj.ejhg.5201402
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- Article
Analysis of TSC2 stop codon variants found in tuberous sclerosis patients.
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- European Journal of Human Genetics, 2001, v. 9, n. 11, p. 823, doi. 10.1038/sj.ejhg.5200728
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- Article
Prediction of BRCA2-association in hereditary breast carcinomas using array-CGH.
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- Breast Cancer Research & Treatment, 2012, v. 132, n. 2, p. 379, doi. 10.1007/s10549-010-1016-7
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- Article
Physical activity and the risk of breast cancer in BRCA1/2 mutation carriers.
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- Breast Cancer Research & Treatment, 2010, v. 120, n. 1, p. 235, doi. 10.1007/s10549-009-0476-0
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- Article
Prediction of BRCA1-association in hereditary non- BRCA1/2 breast carcinomas with array-CGH.
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- Breast Cancer Research & Treatment, 2009, v. 116, n. 3, p. 479, doi. 10.1007/s10549-008-0117-z
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- Article
'We don't know for sure': discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations.
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- Familial Cancer, 2020, v. 19, n. 1, p. 65, doi. 10.1007/s10689-019-00154-4
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- Article
Attitude towards pre-implantation genetic diagnosis for hereditary cancer.
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- Familial Cancer, 2009, v. 8, n. 4, p. 457, doi. 10.1007/s10689-009-9265-5
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- Article
Two TP53 germline mutations in a classical Li-Fraumeni syndrome family.
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- Familial Cancer, 2007, v. 6, n. 3, p. 311, doi. 10.1007/s10689-006-9115-7
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- Article
Late-Onset Common Cancers in a Kindred with an Arg213Gln TP53 Germline Mutation.
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- Familial Cancer, 2006, v. 5, n. 2, p. 169, doi. 10.1007/s10689-005-4789-9
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- Article
Rapid genetic counseling and testing in newly diagnosed breast cancer: Patients’ and health professionals’ attitudes, experiences, and evaluation of effects on treatment decision making.
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- Journal of Surgical Oncology, 2017, v. 116, n. 8, p. 1029, doi. 10.1002/jso.24763
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- Article
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome.
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- Human Mutation, 2016, v. 37, n. 11, p. 1162, doi. 10.1002/humu.23052
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- Article
Behavioral and psychosocial effects of rapid genetic counseling and testing in newly diagnosed breast cancer patients: Design of a multicenter randomized clinical trial.
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- BMC Cancer, 2011, v. 11, n. 1, p. 1, doi. 10.1186/1471-2407-11-6
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- Article