Found: 15
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SEOM recommendations on the structure and operation of hereditary cancer genetic counseling units (HCGCUs).
- Published in:
- Clinical & Translational Oncology, 2013, v. 15, n. 1, p. 20, doi. 10.1007/s12094-012-0920-1
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- Publication type:
- Article
SEOM clinical guidelines for hereditary cancer.
- Published in:
- Clinical & Translational Oncology, 2011, v. 13, n. 8, p. 580, doi. 10.1007/s12094-011-0701-2
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- Publication type:
- Article
Primary lung choriocarcinoma.
- Published in:
- Clinical & Translational Oncology, 2001, v. 3, n. 2, p. 107, doi. 10.1007/BF02711462
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- Publication type:
- Article
Increased Co-Occurrence of Pathogenic Variants in Hereditary Breast and Ovarian Cancer and Lynch Syndromes: A Consequence of Multigene Panel Genetic Testing?
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 19, p. 11499, doi. 10.3390/ijms231911499
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- Publication type:
- Article
Rapid mutation detection in complex genes by heteroduplex analysis with capillary array electrophoresis.
- Published in:
- Electrophoresis, 2005, v. 26, n. 13, p. 2539, doi. 10.1002/elps.200410425
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- Publication type:
- Article
Genetic dissection of the BRCA2 promoter and transcriptional impact of DNA variants.
- Published in:
- Breast Cancer Research & Treatment, 2018, v. 171, n. 1, p. 53, doi. 10.1007/s10549-018-4826-7
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- Publication type:
- Article
Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome in Spain: Clinical and Genetic Characterization.
- Published in:
- Cancers, 2020, v. 12, n. 11, p. 3277, doi. 10.3390/cancers12113277
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- Publication type:
- Article
Germline Genetic Findings Which May Impact Therapeutic Decisions in Families with a Presumed Predisposition for Hereditary Breast and Ovarian Cancer.
- Published in:
- Cancers, 2020, v. 12, n. 8, p. 2151, doi. 10.3390/cancers12082151
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- Publication type:
- Article
KRAS, BRAF, EGFR and HER2 gene status in a Spanish population of colorectal cancer.
- Published in:
- Molecular Biology Reports, 2011, v. 38, n. 2, p. 1315, doi. 10.1007/s11033-010-0232-x
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- Publication type:
- Article
Two founder BRCA2 mutations predispose to breast cancer in young women.
- Published in:
- 2010
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- Publication type:
- Report
Genotype-phenotype correlation in MMR mutation-positive families with Lynch syndrome.
- Published in:
- International Journal of Colorectal Disease, 2013, v. 28, n. 9, p. 1195, doi. 10.1007/s00384-013-1685-x
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- Publication type:
- Article
The highly prevalent BRCA2 mutation c.2808_2811del (3036delACAA) is located in a mutational hotspot and has multiple origins.
- Published in:
- Carcinogenesis, 2013, v. 34, n. 11, p. 2505, doi. 10.1093/carcin/bgt272
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- Publication type:
- Article
Unraveling the molecular effect of a rare missense mutation in BRIP1 associated with inherited breast cancer.
- Published in:
- Molecular Carcinogenesis, 2019, v. 58, n. 1, p. 156, doi. 10.1002/mc.22910
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- Publication type:
- Article
ARID1A genomic alterations driving microsatellite instability through somatic MLH1 methylation with response to immunotherapy in metastatic lung adenocarcinoma: a case report.
- Published in:
- 2021
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- Publication type:
- journal article
A comprehensive custom panel evaluation for routine hereditary cancer testing: improving the yield of germline mutation detection.
- Published in:
- 2020
- By:
- Publication type:
- journal article