Identification of rare intronic variants defining novel BRCA haplotypes

Sanger DNA sequencing is widely used nowadays to identify germ-line alterations of cancer predisposition genes. Molecular diagnosis of hereditary risk of breast and ovarian cancer (HBOC) is mainly targeting BRCA1 and BRCA2, as carriers of deleterious mutations in any of these genes are at significan...

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Bibliographic Details
Main Authors: Anca Negura, Lucian Negura
Format: Article
Language:English
Published: "Alexandru Ioan Cuza" University of Iași 2012-10-01
Series:Analele Ştiinţifice Ale Universităţii Alexandru Ioan Cuza din Iași,Sectiunea II A : Genetica si Biologie Moleculara
Online Access:http://www.gbm.bio.uaic.ro/index.php/gbm/article/view/988