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8. Molecular analysis of human muscular dystrophies. Davies KE; Forrest S; Smith T; Kenwrick S; Ball S; Dorkins H; Patterson M Muscle Nerve; 1987; 10(3):191-9. PubMed ID: 2882417 [TBL] [Abstract][Full Text] [Related]
9. X;autosome translocations in females with Duchenne or Becker muscular dystrophy. Dubowitz V Nature; 1986 Jul 17-23; 322(6076):291-2. PubMed ID: 3461282 [No Abstract] [Full Text] [Related]
10. [Calpain-3 gene defect causing limb gird muscular dystrophy in a Hungarian family]. Horváth R; Walter MC; Lochmüller H; Hübner A; Karcagi V; Pikó H; Timár L; Komoly S Ideggyogy Sz; 2005 Jan; 58(1-2):52-8. PubMed ID: 15884399 [TBL] [Abstract][Full Text] [Related]
11. [Gene hunting of facioscapulohumeral muscular dystrophy]. Song MD; Arahata K No To Shinkei; 1996 Apr; 48(4):307-13. PubMed ID: 8679326 [No Abstract] [Full Text] [Related]
19. Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions. Wijmenga C; van Deutekom JC; Hewitt JE; Padberg GW; van Ommen GJ; Hofker MH; Frants RR Genomics; 1994 Jan; 19(1):21-6. PubMed ID: 7910579 [TBL] [Abstract][Full Text] [Related]
20. Facioscapulohumeral muscular dystrophy: the choice of a biopsy site. Bodensteiner JB; Schochet SS Muscle Nerve; 1986; 9(6):544-7. PubMed ID: 3736585 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]