Haplotype analysis reveals that the recurrent BRCA1 deletion of exons 23 and 24 is a Greek founder mutation-Reference-Cited by-同舟云学术

Haplotype analysis reveals that the recurrent BRCA1 deletion of exons 23 and 24 is a Greek founder mutation

Published:2016-08-22 Issue:3 Volume:91 Page:482-487
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Apostolou P.¹²,Pertesi M.¹³,Aleporou‐Marinou V.²,Dimitrakakis C.⁴,Papadimitriou C.⁵,Razis E.⁶,Christodoulou C.⁷,Fountzilas G.⁸,Yannoukakos D.¹,Konstantopoulou I.¹,Fostira F.¹

Affiliation:

1. Molecular Diagnostics LaboratoryINRaSTES, National Center for Scientific Research “Demokritos” Athens Greece

2. Department of Genetics & Biotechnology, Faculty of BiologyNational and Kapodistrian University of Athens Athens Greece

3. Division of Hematology and Transfusion Medicine, Faculty of Medicine, Department of Laboratory MedicineLund University Lund Sweden

4. Breast Unit of the 1st Department of Obstetrics and GynecologyAthens University Medical School Athens Greece

5. Department of Clinical Therapeutics, "Alexandra" Hospital, School of MedicineUniversity of Athens Athens Greece

6. Third Medical Oncology DepartmentHygeia Hospital Athens Greece

7. Second Department of Medical OncologyMetropolitan Hospital Piraeus Greece

8. School of MedicineAristotle University of Thessaloniki Thessaloniki Greece

Funder

European Social Fund

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.12824

Reference20 articles.

1. A Strong Candidate for the Breast and Ovarian Cancer Susceptibility Gene BRCA1

2. Identification of the breast cancer susceptibility gene BRCA2

3. Gross rearrangements in BRCA1 but not BRCA2 play a notable role in predisposition to breast and ovarian cancer in high-risk families of German origin

4. Genomic rearrangements in BRCA1 and BRCA2: a literature review

5. Large genomic rearrangements of the BRCA1 and BRCA2 genes: review of the literature and report of a novel BRCA1 mutation

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