Early onset facioscapulohumeral muscular dystrophyBROUWER, O. F; PADBERG, G. W; BAKKER, E et al.Muscle & nerve. 1995, pp S67-S72, issn 0148-639X, SUP2Conference Paper

Facioscapulohumeral muscular dystrophy in the dutch populationPADBERG, G. W; FRANTS, R. R; BROUWER, O. F et al.Muscle & nerve. 1995, pp S81-S84, issn 0148-639X, SUP2Conference Paper

Clinical variability of facioscapulohumeral muscular dystrophy in RussiaKAZAKOV, V. M; RUDENKO, D. I.Muscle & nerve. 1995, pp S85-S95, issn 0148-639X, SUP2Conference Paper

The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qterBAKKER, E; WIJMENGA, C; VOSSEN, R. H. A. M et al.Muscle & nerve. 1995, pp S39-S44, issn 0148-639X, SUP2Conference Paper

Monozygotic twins with facioscapulohumeral dystrophy (FSHD) : implications for genotype/phenotype correlationGRIGGS, R. C; TAWIL, R; MCDERMOTT, M et al.Muscle & nerve. 1995, pp S50-S55, issn 0148-639X, SUP2Conference Paper

Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophyLUNT, P. W; JARDINE, P. E; KOCH, M et al.Muscle & nerve. 1995, pp S103-S109, issn 0148-639X, SUP2Conference Paper

Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD)MEENA UPADYAYA; MAYNARD, J; OBSORN, M et al.Muscle & nerve. 1995, pp S45-S49, issn 0148-639X, SUP2Conference Paper

Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD) : immunocytochemical and genetic analysesARAHATA, K; ISHIHARA, T; FUKUNAGA, H et al.Muscle & nerve. 1995, pp S56-S66, issn 0148-639X, SUP2Conference Paper

Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35WIJMENGA, C; DAUWERSE, H. G; PADBERG, G. W et al.Muscle & nerve. 1995, pp S14-S18, issn 0148-639X, SUP2Conference Paper

Mouse myodystrophy (myd) mutation : refined mapping in an interval flanked by homology with distal human 4qMATHEWS, K. D; MILLS, K. A; BAILEY, H. L et al.Muscle & nerve. 1995, pp S98-S102, issn 0148-639X, SUP2Conference Paper

Cloning and mapping of a very short (10-kb) EcoRI fragment associated with faciscapulohumeral muscular dystrophy (FSHD)JE HYEON LEE; GOTO, K; SAHASHI, K et al.Muscle & nerve. 1995, pp S27-S31, issn 0148-639X, SUP2Conference Paper

Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35VAN DEUTEKOM, J. C. T; HOFKER, M. H; ROMBERG, S et al.Muscle & nerve. 1995, pp S19-S26, issn 0148-639X, SUP2Conference Paper