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Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing.
Hum Mutat. 2009 Mar;30(3):472-6. doi: 10.1002/humu.20873.
Hum Mutat. 2009.
PMID: 19058222
Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.
Moens LN, De Rijk P, Reumers J, Van den Bossche MJ, Glassee W, De Zutter S, Lenaerts AS, Nordin A, Nilsson LG, Medina Castello I, Norrback KF, Goossens D, Van Steen K, Adolfsson R, Del-Favero J.
Moens LN, et al. Among authors: glassee w.
PLoS One. 2011;6(8):e23450. doi: 10.1371/journal.pone.0023450. Epub 2011 Aug 11.
PLoS One. 2011.
PMID: 21853134
Free PMC article.
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SNPbox: web-based high-throughput primer design with an eye for repetitive sequences.
Weckx S, De Rijk P, Glassee W, Van Broeckhoven C, Del-Favero J.
Weckx S, et al. Among authors: glassee w.
Methods Mol Biol. 2007;402:179-200. doi: 10.1007/978-1-59745-528-2_9.
Methods Mol Biol. 2007.
PMID: 17951796
Review.
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