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	1.	Biallelicframeshift mutation in RIN2 in a patient with intellectual disability and cataract, without RIN2 syndrome. [electronic resource] by van Amen-Hellebrekers, Claudia J M Jansen, Sandra Stegmann, Alexander P A Stevens, Servi J C Pfundt, Rolph de Vries, Bert B A Producer: 20180621 In: American journal of medical genetics. Part A vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Duplications of SLC1A3: Associated with ADHD and autism. [electronic resource] by van Amen-Hellebrekers, Claudia J M Jansen, Sandra Pfundt, Rolph Schuurs-Hoeijmakers, Janneke H Koolen, David A Marcelis, Carlo L de Leeuw, Nicole de Vries, Bert B A Producer: 20170206 In: European journal of medical genetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Quantification of Phenotype Information Aids the Identification of Novel Disease Genes. [electronic resource] by Vulto-van Silfhout, Anneke T Gilissen, Christian Goeman, Jelle J Jansen, Sandra van Amen-Hellebrekers, Claudia J M van Bon, Bregje W M Koolen, David A Sistermans, Erik A Brunner, Han G de Brouwer, Arjan P M de Vries, Bert B A Producer: 20170629 In: Human mutation vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Clinical significance of de novo and inherited copy-number variation. [electronic resource] by Vulto-van Silfhout, Anneke T Hehir-Kwa, Jayne Y van Bon, Bregje W M Schuurs-Hoeijmakers, Janneke H M Meader, Stephen Hellebrekers, Claudia J M Thoonen, Ilse J M de Brouwer, Arjan P M Brunner, Han G Webber, Caleb Pfundt, Rolph de Leeuw, Nicole de Vries, Bert B A 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)