Authors: Galjaard, RJH Kostakoglu, N Hoogeboom, JJM Breedveld, GJ van der Linde, HC Hovius, SER Oostra, BA Sandkuijl, LA Akarsu, AN Heutink, P

Citation: Rjh. Galjaard et al., X-linked recessive inheritance of radial ray deficiencies in a family withfour affected males, EUR J HUM G, 9(9), 2001, pp. 653-658

Authors: Van Opstal, D van den Berg, C Galjaard, RJH Los, FJ

Citation: D. Van Opstal et al., Follow-up investigations in uncultured amniotic fluid cells after uncertain cytogenetic results, PRENAT DIAG, 21(2), 2001, pp. 75-80

Authors: Kleijer, WJ van Diggelen, OP Keulemans, JLM Losekoot, M Garritsen, VH Stroink, H Majoor-Krakauer, D Franken, PF Eurlings, MCM Taschner, PEM Los, FJ Galjaard, RJH

Citation: Wj. Kleijer et al., First-trimester diagnosis of late-infantile neuronal ceroid lipofuscinosis(LINCL) by tripeptidyl peptidase I assay and CLN2 mutation analysis, PRENAT DIAG, 21(2), 2001, pp. 99-101

Authors: Galjaard, RJH van der Ham, LI Posch, NAS Dijkstra, PF Oostra, BA Hovius, SER Timmenga, EJF Sonneveld, GJ Hoogeboom, AJM Heutink, P

Citation: Rjh. Galjaard et al., Differences in complexity of isolated brachydactyly type C cannot be attributed to locus heterogeneity alone, AM J MED G, 98(3), 2001, pp. 256-262

Authors: van Haelst, MM Hoogeboom, J Galjaard, RJH Kleijer, WJ den Hollander, NS de Krijger, RR Hennekam, RCM Niermeijer, MF

Citation: Mm. Van Haelst et al., Lymphangiectasia with persistent mullerian derivatives: Confirmation of autosomal recessive Urioste syndrome, AM J MED G, 104(1), 2001, pp. 65-68

Authors: van den Berg, C Van Opstal, D Brandenburg, H Wildschut, HIJ den Hollander, NS Pijpers, L Galjaard, RJH Los, FJ

Citation: C. Van Den Berg et al., Accuracy of abnormal karyotypes after the analysis of both short- and long-term culture of chorionic villi, PRENAT DIAG, 20(12), 2000, pp. 956-969