Literature DB >> 17405987

A novel rapid and sensitive BRCA1/2 mutation detection method based on pooled DGGE and targeted sequencing.

P J van Diest, G Pals.   

Abstract

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Year:  2007        PMID： 17405987      PMCID： PMC2001104          DOI： 10.1136/jcp.2006.040501

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN： 0021-9746            Impact factor:   3.411


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  2 in total

1.  A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.

Authors:  Annemarie H van der Hout; Ans M W van den Ouweland; Rob B van der Luijt; Hans J P Gille; Daniëlle Bodmer; Hennie Brüggenwirth; Inge M Mulder; Pieter van der Vlies; Peter Elfferich; Maarten T Huisman; Annelies M ten Berge; Joan Kromosoeto; Rumo P M Jansen; Patrick H A van Zon; Thyrsa Vriesman; Neeltje Arts; Majella Boutmy-de Lange; Jan C Oosterwijk; Hanne Meijers-Heijboer; Margreet G E M Ausems; Nicoline Hoogerbrugge; Senno Verhoef; Dicky J J Halley; Yvonne J Vos; Frans Hogervorst; Marjolijn Ligtenberg; Robert M W Hofstra
Journal:  Hum Mutat       Date:  2006-07       Impact factor: 4.878

2.  A novel BRCA2 mutation in an Indonesian family found with a new, rapid, and sensitive mutation detection method based on pooled denaturing gradient gel electrophoresis and targeted sequencing.

Authors:  D Purnomosari; D K Paramita; T Aryandono; G Pals; P J van Diest
Journal:  J Clin Pathol       Date:  2005-05       Impact factor: 3.411
  2 in total

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