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Results: 1-6 |
Results: 6

Authors: Rosenberg, C Wouters, CH Szuhai, K Dorland, R Pearson, P Poll-The, BT Colombijn, RM Bruning, M Lindhout, D
Citation: C. Rosenberg et al., A Rett syndrome patient with a ring X chromosome: further evidence for skewing of X inactivation and heterogeneity in the aetiology of the disease, EUR J HUM G, 9(3), 2001, pp. 171-177

Authors: Wouters, CH Meijers-Heijboer, HJ Eussen, BJFMM van der Heide, AA van Luijk, RB van Drunen, E Beverloo, BB Visscher, F Van Hemel, JO
Citation: Ch. Wouters et al., Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndrome, AM J MED G, 102(3), 2001, pp. 261-265

Authors: Augustijn, PB Parra, J Wouters, CH Joosten, P Lindhout, D Boas, WV
Citation: Pb. Augustijn et al., Ring chromosome 20 epilepsy syndrome in children: Electroclinical features, NEUROLOGY, 57(6), 2001, pp. 1108-1111

Authors: Versteegh, FGA von Lindern, JS Kemper, J Eichhorn, E Simonsz, HJ Wouters, CH
Citation: Fga. Versteegh et al., Duane retraction syndrome, a new feature in 22q11 deletion syndrome?, CLIN DYSMOR, 9(2), 2000, pp. 135-137

Authors: de Vries, BBA Eussen, BHJ van Diggelen, OP van der Heide, A Deelen, WH Govaerts, LCP Lindhout, D Wouters, CH Van Hemel, JO
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
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