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Editorial

Česká verzia

Published in the journal: Klin Onkol 2016; 29(Supplementum 1): 3
Category: Editorial

Štítky

Paediatric clinical oncology Surgery Clinical oncology

Článek Recommended Extension of Indication Criteria for Genetic Testing of BRCA1 and BRCA2 Mutations in Hereditary Breast and Ovarian Cancer Syndrome

Článek Hereditary Breast and Ovarian Cancer Syndrome

Článek Gynecological Care and Prevention of Gynecological Malignancies in BRCA1 and BRCA2 Mutation Carriers

Článek PALB2 as Another Candidate Gene for Genetic Testing in Patients with Hereditary Breast Cancer in Czech Republic

Článek Retrospective NGS Study in High-risk Hereditary Cancer Patients at Masaryk Memorial Cancer Institute

Článek CZECANCA: CZEch CAncer paNel for Clinical Application – Design and Optimization of the Targeted Sequencing Panel for the Identification of Cancer Susceptibility in High-risk Individuals from the Czech Republic

Článek Genetics of Colorectal Tumorigenesis (Possibilities of Testing and Screening Prediction of Hereditary Form of Colorectal Cancer – Lynch Syndrome)

Článek Syndromes Predisposing to Cancer in Children – the Experience of Pediatric Oncology Departmentof University Hospital Brno

Článek Genetic Syndromes Predisposing to Tumors of Central Nervous System in Children

Článek Hepatoblastoma, Etiology, Case Reports

Článek Identification of a Family with SUFU Germline Deletion Based on a Case of Desmoplastic Medulloblastoma in an Infant

Článek Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene – Case Report

Článok vyšiel v časopise

Clinical Oncology

Číslo Supplementum 1

2016 Číslo Supplementum 1

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