Authors:
Hargrave, M
James, K
Nield, K
Toomes, C
Georgas, K
Sullivan, T
Verzijl, HTFM
Oley, CA
Little, M
De Jonghe, P
Kwon, JM
Kremer, H
Dixon, MJ
Tirnmerman, V
Yamada, T
Koopman, P
Citation: M. Hargrave et al., Fine mapping of the neurally expressed gene SOX14 to human 3q23, relative to three congenital diseases, HUM GENET, 106(4), 2000, pp. 432-439
Authors:
Verzijl, HTFM
van Engelen, BGM
Luyten, JAFM
Steenbergen, GCH
van den Heuvel, LPWJ
ter Laak, HJ
Padberg, GW
Wevers, RA
Citation: Htfm. Verzijl et al., Primary, secondary, and coincidental types of myoadenylate deaminase deficiency - Reply, ANN NEUROL, 45(4), 1999, pp. 548-548
Authors:
Verzijl, HTFM
van den Helm, B
Veldman, B
Hamel, BCJ
Kuyt, LP
Padberg, GW
Kremer, H
Citation: Htfm. Verzijl et al., A second gene for autosomal dominant Mobius syndrome is localized to chromosome 10q, in a Dutch family, AM J HU GEN, 65(3), 1999, pp. 752-756