1. Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium;Sarfarazi, M.; Wijmenga, C.; Upadhyaya, M.;Am Jf Hum Genet,1992
2. Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD);Cacurri, S.; Deidda, G.; Piazzo, N.;Hum Genet,1994
3. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3-3 kb tandemly repeated unit;JCT, Van Deutekom; C, Wijmenga; van Tienhoven EAE;Hum Mol Genet,1993
4. Pulse field gel electrophoresis of the D4F1O4S1 locus reveals the size and the paternal origin of the FSHD-associated deletions;Wijmenga, C.; van Deutekom, J.C.T.; Hewitt, J.E.;Genomics,1994
5. The FSHD locus (pl3E-11) on 4qter shows high homology with 1Oqter;Wijmenga, C.; Bakker, B.; Hofker, M.H.;Muscle Nerve,1994