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Results: 1-7 |
Results: 7
A cascade of complex subtelomeric duplications during the evolution of thehominoid and old world monkey genomes
Authors: van Geel, M Eichler, EE Beck, AF Shan, ZH Haaf, T van der Maarel, SM Frants, RR de Jong, PJ
Citation: M. Van Geel et al., A cascade of complex subtelomeric duplications during the evolution of thehominoid and old world monkey genomes, AM J HU GEN, 70(1), 2002, pp. 269-278
Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysis
Authors: Lernmers, RJLF de Kievit, P van Geel, M van der Wielen, MJR Bakker, E Padberg, GW Frants, RR van der Maarel, SM
Citation: Rjlf. Lernmers et al., Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysis, ANN NEUROL, 50(6), 2001, pp. 816-819
Interchromosomal repeat array interactions between chromosomes 4 and 10: amodel for subtelomeric plasticity
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
De novo facioscapulohumeral muscular dystrophy: Frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10
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
Molecular analysis of facioscapulohumeral muscular dystrophy (FSHD1)
Authors: van der Maarel, SM Bakker, E Frants, RA
Citation: Sm. Van Der Maarel et al., Molecular analysis of facioscapulohumeral muscular dystrophy (FSHD1), METH MOL M, 43, 2000, pp. 305-316
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element
Authors: Gabriels, J Beckers, MC Ding, H De Vriese, A Plaisance, S van der Maarel, SM Padberg, GW Frants, RR Hewitt, JE Collen, D Belayew, A
Citation: J. Gabriels et al., Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element, GENE, 236(1), 1999, pp. 25-32
A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD)
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
Risultati: 1-7 |