Physical Mapping Evidence for a Duplicated Region on Chromosome 10qter Showing High Homology with the Facioscapulohumeral Muscular Dystrophy Locus on Chromosome 4qter

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

D. Pinkel, J. E. Landegent, Colin C. Collins et al. · Proceedings of the National Academy of Sciences · 1988 · 1.3K citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

Cisca Wijmenga, Jane Hewitt, Lodewijk A. Sandkuijl et al. · Nature Genetics · 1992 · 685 citations

Life Sciences, Genetics, Molecular Genetics +16

FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit

Judith C. T. van Deutekom, Cisca Wljmenga, Esther A.E.Van Tlenhoven et al. · Human Molecular Genetics · 1993 · 533 citations

Life Sciences, Genetics, Molecular Genetics +17

Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystropothhy

Jane Hewitt, Robert Lyle, Lorraine N. Clark et al. · Human Molecular Genetics · 1994 · 326 citations

Life Sciences, Genetics, Molecular Genetics +14

The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: Implications for a role of chromatin structure in the pathogenesis of the disease

Sara T. Winokur, Ulla Bengtsson, Julie Feddersen et al. · Chromosome Research · 1994 · 152 citations

Life Sciences, Genetics, Molecular Genetics +13