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	1.	Holoprosencephaly and ZIC2 microdeletions: novel clinical and epidemiological specificities delineated. [electronic resource] by Chabchoub, E Willekens, D Vermeesch, J R Fryns, J-P Producer: 20130703 In: Clinical genetics vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The facial dysmorphy in the newly recognised microdeletion 2p15-p16.1 refined to a 570 kb region in 2p15. [electronic resource] by Chabchoub, E Vermeesch, J R de Ravel, T de Cock, P Fryns, J-P Producer: 20080403 In: Journal of medical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Oculocerebral hypopigmentation syndrome maps to chromosome 3q27.1q29. [electronic resource] by Chabchoub, E Cogulu, O Durmaz, B Vermeesch, J R Ozkinay, F Fryns, J-P Producer: 20120717 In: Dermatology (Basel, Switzerland) vol. 223 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Duplication of the VHL and IRAK2 genes in a patient with mental retardation/multiple congenital anomalies, epilepsy and ectomorphic habitus. [electronic resource] by Chabchoub, E Michils, G Vermeesch, J R De Cock, P Lagae, L Fryns, J P Producer: 20100514 In: Genetic counseling (Geneva, Switzerland) vol. 21 Availability: No items available. Save to lists Add to cart (remove)
	5.	Detection of an unusual 17p13.3 microdeletion by array comparative genomic hybridisation in a patient with lissencephaly. [electronic resource] by Chabchoub, E de Ravel, T Thoelen, R Vermeesch, J R Fryns, J-P Van Esch, H Producer: 20070124 In: Clinical genetics vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)