Found: 20
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Extensive molecular screening for hereditary non-polyposis colorectal cancer.
- Published in:
- 2000
- By:
- Publication type:
- journal article
Reassessing the clinical spectrum associated with hereditary leiomyomatosis and renal cell carcinoma syndrome in French FH mutation carriers.
- Published in:
- Clinical Genetics, 2017, v. 92, n. 6, p. 606, doi. 10.1111/cge.13014
- By:
- Publication type:
- Article
Germline BAP1 mutations predispose also to multiple basal cell carcinomas.
- Published in:
- Clinical Genetics, 2015, v. 88, n. 3, p. 273, doi. 10.1111/cge.12472
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- Publication type:
- Article
Short Report Real-time PCR-based gene dosage assay for detecting BRCA1 rearrangements in breast–ovarian cancer families.
- Published in:
- Clinical Genetics, 2004, v. 65, n. 2, p. 131, doi. 10.1111/j.0009-9163.2004.00200.x
- By:
- Publication type:
- Article
Non-Hodgkin's lymphomas and myeloid disorders: deletions associated with t(2;5) and t(3;5) detected by FISH.
- Published in:
- 1998
- By:
- Publication type:
- journal article
Prise en charge des formes familiales de tumeurs rares : mélanomes familiaux et primitifs multiples.
- Published in:
- Oncologie (Tech Science Press), 2008, v. 10, n. 6, p. 411, doi. 10.1007/s10269-008-0906-3
- By:
- Publication type:
- Article
Prédisposition génétique aux cancers du sein et de l’ovaire: Diagnostic moléculaire et conséquences.
- Published in:
- Oncologie (Tech Science Press), 2006, v. 8, n. 3, p. 213, doi. 10.1007/s10269-006-0361-y
- By:
- Publication type:
- Article
Subungual squamous cell carcinoma in a BAP1 germline pathogenic variant carrier.
- Published in:
- Journal of the European Academy of Dermatology & Venereology, 2021, v. 35, n. 10, p. e665, doi. 10.1111/jdv.17372
- By:
- Publication type:
- Article
Contribution of CDKN2A/P16, P14, CDK4 and BRCA1/2 germline mutations in individuals with suspected genetic predisposition to uveal melanoma.
- Published in:
- Familial Cancer, 2010, v. 9, n. 4, p. 663, doi. 10.1007/s10689-010-9379-9
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- Publication type:
- Article
Prevalence of the E318 K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history.
- Published in:
- Pigment Cell & Melanoma Research, 2013, v. 26, n. 2, p. 259, doi. 10.1111/pcmr.12047
- By:
- Publication type:
- Article
The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Mutations in BHD and TP53 genes, but not in HNF1β gene, in a large series of sporadic chromophobe renal cell carcinoma.
- Published in:
- 2007
- By:
- Publication type:
- Correction Notice
Mutations in BHD and TP53 genes, but not in HNF1β gene, in a large series of sporadic chromophobe renal cell carcinoma.
- Published in:
- British Journal of Cancer, 2007, v. 96, n. 2, p. 336, doi. 10.1038/sj.bjc.6603492
- By:
- Publication type:
- Article
Search for germline alterations in CDKN2A/ARF and CDK4 of 42 Jewish melanoma families with or without neural system tumours.
- Published in:
- 2005
- By:
- Publication type:
- journal article
P53 germline mutations in childhood cancers and cancer risk for carrier individuals.
- Published in:
- British Journal of Cancer, 2000, v. 82, n. 12, p. 1932
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- Publication type:
- Article
Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16<sup>INK4A</sup>, P14<sup>ARF</sup> or cdk4 genes.
- Published in:
- British Journal of Cancer, 2000, v. 82, n. 4, p. 818, doi. 10.1054/bjoc.1999.1005
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- Publication type:
- Article
Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families.
- Published in:
- British Journal of Cancer, 1999, v. 80, n. 7, p. 1042, doi. 10.1038/sj.bjc.6690460
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- Publication type:
- Article
Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2010, v. 102, n. 20, p. 1568, doi. 10.1093/jnci/djq363
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- Publication type:
- Article
Genital and anorectal mucosal melanoma is associated with cutaneous melanoma in patients and in families.
- Published in:
- British Journal of Dermatology, 2013, v. 169, n. 3, p. 594, doi. 10.1111/bjd.12421
- By:
- Publication type:
- Article
Novel FH mutation in a patient with cutaneous leiomyomatosis associated with cutis verticis gyrata, eruptive collagenoma and Charcot-Marie-Tooth disease M. Marque et al. Novel FH mutation.
- Published in:
- British Journal of Dermatology, 2010, v. 163, n. 6, p. 1337, doi. 10.1111/j.1365-2133.2010.09912.x
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- Publication type:
- Article