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	1.	Flexible, scalable, and efficient targeted resequencing on a benchtop sequencer for variant detection in clinical practice. [electronic resource] by De Leeneer, Kim Hellemans, Jan Steyaert, Wouter Lefever, Steve Vereecke, Inge Debals, Eveline Crombez, Brecht Baetens, Machteld Van Heetvelde, Mattias Coppieters, Frauke Vandesompele, Jo De Jaegher, Annelies De Baere, Elfride Coucke, Paul Claes, Kathleen Producer: 20151125 In: Human mutation vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Identity-by-descent-guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy. [electronic resource] by Coppieters, Frauke Van Schil, Kristof Bauwens, Miriam Verdin, Hannah De Jaegher, Annelies Syx, Delfien Sante, Tom Lefever, Steve Abdelmoula, Nouha Bouayed Depasse, Fanny Casteels, Ingele de Ravel, Thomy Meire, Françoise Leroy, Bart P De Baere, Elfride Producer: 20150522 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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