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Citation: A. Verloes et al., Major decrease in the incidence of trisomy21 at birth in south Belgium: mass impact of triple test?, EUR J HUM G, 9(1), 2001, pp. 1-4

Authors: De Baere, E Dixon, MJ Small, KW Jabs, EW Leroy, BP Devriendt, K Gillerot, Y Mortier, G Meire, F Van Maldergem, L Courtens, W Hjalgrim, H Huang, S Liebaers, I Van Regemorter, N Touraine, P Praphanphoj, V Verloes, A Udar, N Yellore, V Chalukya, M Yelchits, S De Paepe, A Kuttenn, F Fellous, M Veitia, R Messiaen, L

Citation: E. De Baere et al., Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation, HUM MOL GEN, 10(15), 2001, pp. 1591-1600

Authors: Jauniaux, E Gillerot, Y Hustin, J

Citation: E. Jauniaux et al., Placental and fetal cancers, CANCER AND PREGNANCY, 2001, pp. 6-20

Authors: Van Maldergem, L Tuerlinckx, D Wanders, RJ Vianey-Saban, C Van Hoof, F Martin, JJ Fourneau, C Gillerot, Y Bachy, A

Citation: L. Van Maldergem et al., Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and early-onset liver cirrhosis in two siblings, EUR J PED, 159(1-2), 2000, pp. 108-112

Authors: Silva, ES Lumbroso, S Medina, M Gillerot, Y Sultan, C Sokal, EM

Citation: Es. Silva et al., Demonstration of McCune-Albright mutations in the liver of children with high gamma GT progressive cholestasis, J HEPATOL, 32(1), 2000, pp. 154-158