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Neurology, Vol. 68, Issue 8, 544-545, February 20, 2007

EDITORIALS

Pushing the genetic frontier with facioscapulohumeral muscular dystrophy

Steven A. Greenberg and George W. Padberg

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February 20 Highlights
Neurology 2007 68: 540-541. [Full Text] [PDF]

Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy
R. J. Osborne, S. Welle, S. L. Venance, C. A. Thornton, and R. Tawil
Neurology 2007 68: 569-577. [Abstract] [Full Text] [PDF]

Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4
K. L. Deak, R. J.L.F Lemmers, J. M. Stajich, R. Klooster, R. Tawil, R. R. Frants, M. C. Speer, S. M. van der Maarel, and J. R. Gilbert
Neurology 2007 68: 578-582. [Abstract] [Full Text] [PDF]




This Article
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Google Scholar
Right arrow Articles by Greenberg, S. A.
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PubMed
Right arrow PubMed Citation
Right arrow Articles by Greenberg, S. A.
Right arrow Articles by Padberg, G. W.
Related Collections
Right arrow Muscle disease
Right arrow Retina
Right arrow Gene expression studies
Right arrow All Genetics
Right arrowRelated Articles