Authors: Rosias, PPR Sijstermans, JMJ Theunissen, PMVM Pulles-Heintzberger, CFM De Die-Smulders, CEM Engelen, JJM Van Der Meer, SB

Citation: Ppr. Rosias et al., Phenotypic variability of the cat eye syndrome. Case report and review of the literature, GEN COUNSEL, 12(3), 2001, pp. 273-282

Authors: Moog, U De Die-Smulders, CEM Schrander-Stumpel, CTRM Engelen, JJM Hamers, AJH Frints, S Fryns, JP

Citation: U. Moog et al., Holoprosencephaly: The Maastricht experience, GEN COUNSEL, 12(3), 2001, pp. 287-298

Authors: Mertens, DJLM De Die-Smulders, CEM Kampschoer, PHNM Offermans, JPM Engelen, JJM Hamers, AJH Lammens, M Schrander-Stumpel, CTRM

Citation: Djlm. Mertens et al., 14q terminal deletion: Prenatal diagnosis in a child with severe congenital anomalies, GEN COUNSEL, 11(4), 2000, pp. 341-346

Authors: Engelen, JJM Tuerlings, JHAM Albrechts, JCM Schrander-Stumpel, CTRM Hamers, AJH De Die-Smulders, CEM

Citation: Jjm. Engelen et al., Prenatally detected marker chromosome identified as an i(22)(p10) using (micro)FISH, GEN COUNSEL, 11(1), 2000, pp. 13-17

Authors: Engelen, JJM De Die-Smulders, CEM Vos, PTH Meers, LEC Albrechts, JCM Hamers, AJH

Citation: Jjm. Engelen et al., Characterization of a partial trisomy 16q with fish - Report of a patient and review of the literature, ANN GENET, 42(2), 1999, pp. 101-104