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	1.	Shah-Waardenburg syndrome and PCWH associated with SOX10 mutations: a case report and review of the literature. [electronic resource] by Verheij, Johanna B G M Sival, Deborah A van der Hoeven, Johannes H Vos, Yvonne J Meiners, Linda C Brouwer, Oebele F van Essen, Anthonie J Producer: 20060621 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Whole-exome sequencing is a powerful approach for establishing the etiological diagnosis in patients with intellectual disability and microcephaly. [electronic resource] by Rump, Patrick Jazayeri, Omid van Dijk-Bos, Krista K Johansson, Lennart F van Essen, Anthonie J Verheij, Johanna B G M Veenstra-Knol, Hermine E Redeker, Egbert J W Mannens, Marcel M A M Swertz, Morris A Alizadeh, Behrooz Z van Ravenswaaij-Arts, Conny M A Sinke, Richard J Sikkema-Raddatz, Birgit Producer: 20160930 In: BMC medical genomics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformations. [electronic resource] by D'haene, Barbara Meire, Françoise Claerhout, Ilse Kroes, Hester Y Plomp, Astrid Arens, Yvonne H de Ravel, Thomy Casteels, Ingele De Jaegere, Sarah Hooghe, Sally Wuyts, Wim van den Ende, Jenneke Roulez, Françoise Veenstra-Knol, Hermine E Oldenburg, Rogier A Giltay, Jacques Verheij, Johanna B G M de Faber, Jan-Tjeerd Menten, Björn De Paepe, Anne Kestelyn, Philippe Leroy, Bart P De Baere, Elfride Producer: 20110225 In: Investigative ophthalmology & visual science vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)