Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH-Reference-Cited by-同舟云学术

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Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH

Published:2005-06 Issue:2 Volume:4 Page:145-149
ISSN:1389-9600
Container-title:Familial Cancer
language:en
Short-container-title:Familial Cancer

Author:

Akrami Seyed Mohammad,Dunlop Malcolm G.,Farrington Susan M.,Frayling Ian M.,MacDonald Fiona,Harvey John F.,Armour John A. L.

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics (clinical),Oncology,Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10689-004-6131-3.pdf

Reference14 articles.

1. MSH2 genomic deletions are a frequent cause of HNPCC

2. Measurement of locus copy number by hybridisation with amplifiable probes

3. High throughput screening of human subtelomeric DNA for copy number changes using multiplex amplifiable probe hybridisation (MAPH)

4. Detection of a large TBX5 deletion in a family with Holt-Oram syndrome

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1. All y’all need to know ‘bout retroelements in cancer;Seminars in Cancer Biology;2010-08

2. Exon deletions of the phenylalanine hydroxylase gene in Italian hyperphenylalaninemics;Experimental and Molecular Medicine;2010

3. Quadruplex MAPH: improvement of throughput in high-resolution copy number screening;BMC Genomics;2009-09-28

4. New applications and developments in the use of multiplex ligation-dependent probe amplification;ELECTROPHORESIS;2008-12

5. Molecular diagnosis utility of multiplex ligation-dependent probe amplification;Expert Opinion on Medical Diagnostics;2008-04

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