Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR–based GS‐FLX sequencing
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P. D. Rijk | L. Moens | E. Nelis | J. Del-Favero | P. Jonghe | An-Sofie Lenaerts | D. Goossens | A. Kalbe | B. Frey | G. Kopal | Wim Glassee | An‐Sofie Lenaerts | P. Rijk | Andreas Kalbe