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Muscle & Nerve. Supplement|January 1, 1995
Leber's hereditary optic neuropathy among JapaneseS Ishikawa, Y Ichibe, J Yokoe, et al.Muscle & Nerve. Supplement|January 1, 1995
Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD)J H Lee, K Goto, K Sahashi, et al.Muscle & Nerve. Supplement|January 1, 1995
Efforts toward understanding the molecular basis of facioscapulohumeral muscular dystrophyM R Altherr, U Bengtsson, R P Markovich, et al.Muscle & Nerve. Supplement|January 1, 1995
Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, J Maynard, M Osborn, et al.Muscle & Nerve. Supplement|January 1, 1995
Monozygotic twins with facioscapulohumeral dystrophy (FSHD): implications for genotype/phenotype correlation. FSH-DY GroupR C Griggs, R Tawil, M McDermott, et al.Muscle & Nerve. Supplement|January 1, 1995
Facioscapulohumeral muscular dystrophy in the Dutch populationG W Padberg, R R Frants, O F Brouwer, et al.Muscle & Nerve. Supplement|April 12, 2013
Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD)M Upadhyaya, J Maynard, M Osborn, et al.Muscle & Nerve. Supplement|April 12, 2013
Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analysesK Arahata, T Ishihara, H Fukunaga, et al.Muscle & Nerve. Supplement|April 12, 2013
Early onset facioscapulohumeral muscular dystrophyO F Brouwer, G W Padberg, E Bakker, et al.Muscle & Nerve. Supplement|April 12, 2013
On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophyG W Padberg, O F Brouwer, R J de Keizer, et al.Pageof 11