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Citation: J. Celli et al., Familial syndromic esophageal atresia maps to 2p23-p24, AM J HU GEN, 66(2), 2000, pp. 436-444

Authors: De Krijger, RR Mooy, CM Van Hemel, JO Sulkers, EJ Kros, JM Bartelings, MM Govaerts, LCP

Citation: Rr. De Krijger et al., CHARGE association-related ocular pathology in a newborn with partial trisomy 19q and partial monosomy 21q, from a maternal translocation (19;21) (q13.1;q22.3), PEDIATR D P, 2(6), 1999, pp. 577-581

Authors: Giltay, JC Kastrop, PMM Tuerlings, JHAM Kremer, JAM Tiemessen, CHJ Gerssen-Schoorl, KBJ van der Veen, F de Vries, J Hordijk, R Hamers, GJH Hansson, K van der Blij-Philipsen, M Govaerts, LCP Pieters, MHEC Madan, K Scheres, JMJC

Citation: Jc. Giltay et al., Subfertile men with constitutive chromosome abnormalities do not necessarily refrain from intracytoplasmic sperm injection treatment: a follow-up study on 75 Dutch patients, HUM REPR, 14(2), 1999, pp. 318-320

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Citation: Bba. De Vries et al., Submicroscopic xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14), AM J MED G, 87(2), 1999, pp. 189-194

Authors: Wouters, CH Van Bodegom, TM Moll, HA Govaerts, LCP

Citation: Ch. Wouters et al., Partial trisomy 4q and monosomy 9p resulting from a familial translocationt(4;9)(q27;p24) in a child with choanal atresia, ANN GENET, 42(3), 1999, pp. 160-165