Authors:
Leegwater, PAJ
Vermeulen, G
Konst, AAM
Naidu, S
Mulders, J
Visser, A
Kersbergen, P
Mobach, D
Fonds, D
van Berkel, CGM
Lemmers, RJLF
Frants, RR
Oudejans, CBM
Schutgens, RBH
Pronk, JC
van der Knaap, MS
Citation: Paj. Leegwater et al., Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter, NAT GENET, 29(4), 2001, pp. 383-388
Authors:
van Geel, M
van Deutekom, JCT
van Staalduinen, A
Lemmers, RJLF
Dickson, MC
Hofker, MH
Padberg, GW
Hewitt, JE
de Jong, PJ
Frants, RR
Citation: M. Van Geel et al., Identification of a novel beta-tubulin subfamily with one member (TUBB4Q) located near the telomere of chromosome region 4q35, CYTOG C GEN, 88(3-4), 2000, pp. 316-321
Authors:
van der Maarel, SM
Deidda, G
Lemmers, RJLF
van Overveld, PGM
van der Wielen, M
Hewitt, JE
Sandkuijl, L
Bakker, B
van Ommen, GJB
Padberg, GW
Frants, RR
Citation: Sm. Van Der Maarel et al., De novo facioscapulohumeral muscular dystrophy: Frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10, AM J HU GEN, 66(1), 2000, pp. 26-35
Authors:
van der Maarel, SM
Deidda, G
Lemmers, RJLF
Bakker, E
van der Wielen, MJR
Sandkuijl, L
Hewitt, JE
Padberg, GW
Frants, RR
Citation: Sm. Van Der Maarel et al., A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD), J MED GENET, 36(11), 1999, pp. 823-828