Authors: Verloes, A Gillerot, Y Van Maldergem, L Schoos, R Herens, C Jamar, M Dideberg, V Lesenfants, S Koulischer, L

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: Scantamburlo, G Lampertz, S Croisiau, C Jamar, M Koulischer, L Herens, C

Citation: G. Scantamburlo et al., Inv(12)(q15q24): A nonrandom change associated with myelodysplasia?, CANC GENET, 121(2), 2000, pp. 206-207

Authors: Herens, C Tassin, F Lemaire, V Beguin, Y Collard, E Lampertz, S Croisiau, C Lecomte, M De Prijk, B Longree, L Koulischer, L

Citation: C. Herens et al., Deletion of the 5 '-ABL region: a recurrent anomaly detected by fluorescence in situ hybridization in about 10% of Philadelphia-positive chronic myeloid leukaemia patients, BR J HAEM, 110(1), 2000, pp. 214-216

Authors: Poncin, J Abs, R Velkeniers, B Bonduelle, M Abramowicz, M Legros, JJ Verloes, A Meurisse, M Van Gaal, L Verellen, C Koulischer, L Beckers, A

Citation: J. Poncin et al., Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases, HUM MUTAT, 13(1), 1999, pp. 54-60

Authors: Herens, C Hermanne, JP Tassin, F Fassotte, MF Thiry, A Jamar, M Schaaf-Lafontaine, N Fillet, G Koulischer, L

Citation: C. Herens et al., Translocation (2;3)(p21;q26) as the sole anomaly in a case of primary myelofibrosis, CANC GENET, 110(1), 1999, pp. 62-64

Authors: Herens, C Brasseur, E Jamar, M Vierset, L Schoenen, I Koulischer, L

Citation: C. Herens et al., Loss of the Y chromosome in bone marrow cells: results on 1907 consecutivecases of leukaemia and preleukaemia, CLIN LAB H, 21(1), 1999, pp. 17-20