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	1.	De novo mutations of SETBP1 cause Schinzel-Giedion syndrome. [electronic resource] by Hoischen, Alexander van Bon, Bregje W M Gilissen, Christian Arts, Peer van Lier, Bart Steehouwer, Marloes de Vries, Petra de Reuver, Rick Wieskamp, Nienke Mortier, Geert Devriendt, Koen Amorim, Marta Z Revencu, Nicole Kidd, Alexa Barbosa, Mafalda Turner, Anne Smith, Janine Oley, Christina Henderson, Alex Hayes, Ian M Thompson, Elizabeth M Brunner, Han G de Vries, Bert B A Veltman, Joris A Producer: 20100617 In: Nature genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A post-hoc comparison of the utility of sanger sequencing and exome sequencing for the diagnosis of heterogeneous diseases. [electronic resource] by Neveling, Kornelia Feenstra, Ilse Gilissen, Christian Hoefsloot, Lies H Kamsteeg, Erik-Jan Mensenkamp, Arjen R Rodenburg, Richard J T Yntema, Helger G Spruijt, Liesbeth Vermeer, Sascha Rinne, Tuula van Gassen, Koen L Bodmer, Danielle Lugtenberg, Dorien de Reuver, Rick Buijsman, Wendy Derks, Ronny C Wieskamp, Nienke van den Heuvel, Bert Ligtenberg, Marjolijn J L Kremer, Hannie Koolen, David A van de Warrenburg, Bart P C Cremers, Frans P M Marcelis, Carlo L M Smeitink, Jan A M Wortmann, Saskia B van Zelst-Stams, Wendy A G Veltman, Joris A Brunner, Han G Scheffer, Hans Nelen, Marcel R Producer: 20140616 In: Human mutation vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)