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25. Molecular diagnosis of facioscapulohumeral muscular dystrophy. Upadhyaya M; Cooper DN Expert Rev Mol Diagn; 2002 Mar; 2(2):160-71. PubMed ID: 11962336 [TBL] [Abstract][Full Text] [Related]
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32. Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4. Deak KL; Lemmers RJ; Stajich JM; Klooster R; Tawil R; Frants RR; Speer MC; van der Maarel SM; Gilbert JR Neurology; 2007 Feb; 68(8):578-82. PubMed ID: 17229919 [TBL] [Abstract][Full Text] [Related]
33. A Unique Case of Type-1 Facioscapulohumeral Muscular Dystrophy and Sarcomeric Hypertrophic Cardiomyopathy. Lima da Silva G; GuimarĂ£es T; Pinto FJ; Brito D Rev Esp Cardiol (Engl Ed); 2018 Sep; 71(9):765-766. PubMed ID: 28697927 [No Abstract] [Full Text] [Related]
34. Facioscapulohumeral muscular dystrophy presenting isolated monomelic lower limb atrophy. Report of two patients with and without 4q35 rearrangement. Uncini A; Galluzzi G; Di Muzio A; De Angelis MV; Ricci E; Scoppetta C; Servidei S Neuromuscul Disord; 2002 Nov; 12(9):874-7. PubMed ID: 12398841 [TBL] [Abstract][Full Text] [Related]
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