Authors: van Overveld, PGM Lemmers, RJFL Deidda, G Sandkuijl, L Padberg, GW Frants, RR van der Maarel, SM

Citation: Pgm. Van Overveld et al., Interchromosomal repeat array interactions between chromosomes 4 and 10: amodel for subtelomeric plasticity, HUM MOL GEN, 9(19), 2000, pp. 2879-2884

Authors: Feroci, M Orlando, L Balia, R Bosman, C Cardarelli, E Deidda, G

Citation: M. Feroci et al., Some considerations on shallow seismic reflection surveys, J APP GEOPH, 45(2), 2000, pp. 127-139

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: Galluzzi, G Deidda, G Cacurri, S Colantoni, L Piazzo, N Vigneti, E Ricci, E Servidei, S Merico, B Pachi, A Brambati, B Mangiola, F Tonali, P Felicetti, L

Citation: G. Galluzzi et al., Molecular analysis of 4q35 rearrangements in facioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease, NEUROMUSC D, 9(3), 1999, pp. 190-198

Authors: Ricci, E Galluzzi, G Deidda, G Cacurri, S Colantoni, L Merico, B Piazzo, N Servidei, S Vigneti, E Pasceri, V Silvestri, G Mirabella, M Mangiola, F Tonali, P Felicetti, L

Citation: E. Ricci et al., Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype, ANN NEUROL, 45(6), 1999, pp. 751-757

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