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Facioscapulohumeral muscular dystrophy in early childhood.
Brouwer OF, Padberg GW, Wijmenga C, Frants RR. Brouwer OF, et al. Among authors: frants rr. Arch Neurol. 1994 Apr;51(4):387-94. doi: 10.1001/archneur.1994.00540160085011. Arch Neurol. 1994. PMID: 8155016 Review.
Molecular genetics of facioscapulohumeral muscular dystrophy.
Wijmenga C, Frants RR, Hewitt JE, van Deutekom JC, van Geel M, Wright TJ, Padberg GW, Hofker MH, van Ommen GJ. Wijmenga C, et al. Among authors: frants rr. Neuromuscul Disord. 1993 Sep-Nov;3(5-6):487-91. doi: 10.1016/0960-8966(93)90102-p. Neuromuscul Disord. 1993. PMID: 8186699 Review.
De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10.
van der Maarel SM, Deidda G, Lemmers RJ, van Overveld PG, van der Wielen M, Hewitt JE, Sandkuijl L, Bakker B, van Ommen GJ, Padberg GW, Frants RR. van der Maarel SM, et al. Among authors: frants rr. Am J Hum Genet. 2000 Jan;66(1):26-35. doi: 10.1086/302730. Am J Hum Genet. 2000. PMID: 10631134 Free PMC article.
407 results