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Results: 4

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
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