M J van der Wielen

Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases.

Egbert Bakker, M J van der Wielen, Els Voorhoeve et al. · Journal of Medical Genetics · 1996 · 61 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD)

Silvère M. van der Maarel, Giancarlo Deidda, R. J. L. F. Lemmers et al. · Journal of Medical Genetics · 1999 · 40 citations

Life Sciences, Genetics, Molecular Genetics +17

Possible phenotypic dosage effect in patients compound heterozygous for FSHD-sized 4q35 alleles

M. Wohlgemuth, R. Lemmers, E.L. van der Kooi et al. · Neurology · 2003 · 32 citations

Life Sciences, Genetics, Molecular Genetics +17

Refinement of the localisation of the X linked keratosis follicularis spinulosa decalvans (KFSD) gene in Xp22.13-p22.2.

Jan C. Oosterwijk, M J van der Wielen, Esther van de Vosse et al. · Journal of Medical Genetics · 1995 · 25 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11