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Literature DB >> 11106360

2157delG: a frequent mutation in BRCA2 missed by PTT.

J F Davies, E K Redmond, M C Cox, F I Lalloo, R Elles, D G Evans.

Abstract

Entities: Gene Mutation

Mesh：

Substances：

Year: 2000 PMID： 11106360 PMCID： PMC1734498 DOI： 10.1136/jmg.37.12.e42

Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318

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4 in total

1. High detection rate for BRCA2 mutations in male breast cancer families from North West England.

Authors: D G Evans; M Bulman; K Young; D Gokhale; F Lalloo
Journal: Fam Cancer Date: 2001 Impact factor: 2.375

2. Screening human genes for small alterations performing an enzymatic cleavage mismatched analysis (ECMA) protocol.

Authors: Nikolaos Vogiatzakis; Kyriaki Kekou; Christalena Sophocleous; Sophia Kitsiou; Ariadni Mavrou; Chrisa Bakoula; Emmanouel Kanavakis
Journal: Mol Biotechnol Date: 2007-08-03 Impact factor: 2.695

3. BRCA1/2 mutation analysis in male breast cancer families from North West England.

Authors: D G R Evans; Mike Bulman; Karen Young; Emma Howard; Stuart Bayliss; Andrew Wallace; Fiona Lalloo
Journal: Fam Cancer Date: 2007-07-17 Impact factor: 2.375

4. Screening human genes for small alterations performing an enzymatic cleavage mismatched analysis (ECMA) protocol.

4 in total