Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing-Reference-Cited by-同舟云学术

Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing

Published:2008-12-04 Issue:3 Volume:30 Page:472-476
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Goossens Dirk,Moens Lotte N.,Nelis Eva,Lenaerts An-Sofie,Glassee Wim,Kalbe Andreas,Frey Bruno,Kopal Guido,Jonghe Peter De,Rijk Peter De,Del-Favero Jurgen

Funder

Industrial Research Fund of the University of Antwerp (IOF)

Research Foundation-Flanders (FWO)

Institute for the Promotion of Innovation through Science and Technology in Flanders (IWT)

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference22 articles.

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4. Multiplex PCR: advantages, development, and applications;Edwards;PCR Methods Appl,1994

5. Multiplex PCR: optimization and application in diagnostic virology;Elnifro;Clin Microbiol Rev,2000

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