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: Martin, JJ Van Regemorter, N Del-Favero, J Lofgren, A Van Broeckhoven, C

Citation: Jj. Martin et al., Spinocerebellar ataxia type 7 (SCA7) - correlations between phenotype and genotype in one large Belgian family, J NEUR SCI, 168(1), 1999, pp. 37-46

Authors: Reyniers, E Van Bogaert, P Peeters, N Vits, L Pauly, F Fransen, E Van Regemorter, N Kooy, RF

Citation: E. Reyniers et al., A new neurological syndrome with mental retardation, choreoathetosis, and abnormal behavior maps to chromosome Xp11, AM J HU GEN, 65(5), 1999, pp. 1406-1412

Authors: Wetzburger, CL Van Regemorter, N Szliwowski, HB Abramowicz, MJ Van Bogaert, P

Citation: Cl. Wetzburger et al., Gray matter heterotopia and acute necrotizing encephalopathy in trichothiodystrophy, PED NEUROL, 19(5), 1998, pp. 392-394