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:
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