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	1.	Discordant monozygotic twins for macrocephaly-capillary malformation. [electronic resource] by Lederer, Damien Rack, Katrina Boulanger, Sébastien Battisti, Oreste Verellen-Dumoulin, Christine Producer: 20120924 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Role of CGH array in the diagnosis of autosomal recessive disease: a case of Ellis-van Creveld syndrome. [electronic resource] by D'Ambrosio, Valentina Votino, Carmela Cos, Teresa Boulanger, Sebastien Dheedene, Annelies Jani, Jacques Keymolen, Kathelijn Producer: 20151230 In: Prenatal diagnosis vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Expanding phenotype of p.Ala140Val mutation in MECP2 in a 4 generation family with X-linked intellectual disability and spasticity. [electronic resource] by Lambert, Sophie Maystadt, Isabelle Boulanger, Sébastien Vrielynck, Pascal Destrée, Anne Lederer, Damien Moortgat, Stéphanie Producer: 20170207 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)
	4.	Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy. [electronic resource] by Moortgat, Stéphanie Désir, Julie Benoit, Valérie Boulanger, Sébastien Pendeville, Hélène Nassogne, Marie-Cécile Lederer, Damien Maystadt, Isabelle Producer: 20171019 In: American journal of medical genetics. Part A vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Trisomy rescue mechanism: the case of concomitant mosaic trisomy 14 and maternal uniparental disomy 14 in a 15-year-old girl. [electronic resource] by Balbeur, Samuel Grisart, Bernard Parmentier, Benoit Sartenaer, Daniel Leonard, Pierre-Emmanuel Ullmann, Urielle Boulanger, Sébastien Leroy, Luc Ngendahayo, Placide Lungu-Silviu, Constantin Lysy, Philippe Maystadt, Isabelle Producer: 20160325 In: Clinical case reports vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Expanding the phenotypic spectrum associated with OPHN1 mutations: Report of 17 individuals with intellectual disability but no cerebellar hypoplasia. [electronic resource] by Moortgat, Stéphanie Lederer, Damien Deprez, Marie Buzatu, Marga Clapuyt, Philippe Boulanger, Sébastien Benoit, Valérie Mary, Sandrine Guichet, Agnès Ziegler, Alban Colin, Estelle Bonneau, Dominique Maystadt, Isabelle Producer: 20190321 In: European journal of medical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)