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	1.	Cri du chat syndrome: changing phenotype in older patients. [electronic resource] by Van Buggenhout, G J Pijkels, E Holvoet, M Schaap, C Hamel, B C Fryns, J P Producer: 20000301 In: American journal of medical genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A genetic diagnostic survey in an institutionalized population of 116 moderately to severely retarded male patients: the Rekem experience. [electronic resource] by Schaap, C Schrander-Stumpel, C T Colla-Pijkels, E T Van Driessche, J Kusters, R Fryns, J P Producer: 19960325 In: Genetic counseling (Geneva, Switzerland) vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	3.	Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD). [electronic resource] by Debeer, Ph Van Esch, H Huysmans, C Pijkels, E De Smet, L Van de Ven, W Devriendt, K Fryns, J-P Producer: 20060228 In: European journal of medical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophy. [electronic resource] by Steyaert, J Umans, S Willekens, D Legius, E Pijkels, E de Die-Smulders, C Van den Berghe, H Fryns, J P Producer: 19971107 In: Clinical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Fountain syndrome: further delineation of the clinical syndrome and follow-up data. [electronic resource] by Van Buggenhout, G J Van Ravenswaaij-Arts, C M Renier, W O Van de Wiel, M P Trommelen, J C Pijkels, E Hamel, B C Fryns, J P Producer: 19970303 In: Genetic counseling (Geneva, Switzerland) vol. 7 Availability: No items available. Save to lists Add to cart (remove)