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4. The facio-scapulo-limb (or the facioscapulohumeral) type of muscular dystrophy. Clinical and genetic study of 200 cases. Kazakov VM; Bogorodinsky DK; Znoyko ZV; Skorometz AA Eur Neurol; 1974; 11(4):236-60. PubMed ID: 4854830 [No Abstract] [Full Text] [Related]
5. Linkage studies in facioscapulohumeral muscular dystrophy. Padberg GW; Klasen EC; Volkers WS; De Lange GG; Wintzen AR Muscle Nerve; 1988 Aug; 11(8):833-5. PubMed ID: 3140007 [TBL] [Abstract][Full Text] [Related]
6. Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD). Gilbert JR; Stajich JM; Wall S; Carter SC; Qiu H; Vance JM; Stewart CS; Speer MC; Pufky J; Yamaoka LH Am J Hum Genet; 1993 Aug; 53(2):401-8. PubMed ID: 8328457 [TBL] [Abstract][Full Text] [Related]
7. Evidence against location of the gene for facioscapulohumeral muscular dystrophy on the distal long arm of chromosome 14. Lunt PW; Noades JG; Upadhyaya M; Sarfarazi M; Harper PS J Neurol Sci; 1988 Dec; 88(1-3):287-92. PubMed ID: 3225626 [TBL] [Abstract][Full Text] [Related]
8. The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD). Upadhyaya M; Lunt P; Sarfarazi M; Broadhead W; Farnham J; Harper PS Am J Hum Genet; 1992 Aug; 51(2):404-10. PubMed ID: 1642238 [TBL] [Abstract][Full Text] [Related]
9. A clinically homogeneous group of families with facioscapulohumeral (Landouzy-Déjérine) muscular dystrophy: linkage analysis of six autosomes. Jacobsen SJ; Diala ES; Dorsey BV; Rising MB; Graveline R; Falls K; Schultz P; Hogan C; Rediker K; D'Amico C Am J Hum Genet; 1990 Sep; 47(3):376-88. PubMed ID: 1975474 [TBL] [Abstract][Full Text] [Related]
18. Facioscapulohumeral muscular dystrophy gene in Dutch families is not linked to markers for familial adenomatous polyposis on the long arm of chromosome 5. Wijmenga C; Frants RR; Brouwer OF; van der Klift HM; Meera Khan P; Padberg GW J Neurol Sci; 1990 Feb; 95(2):225-9. PubMed ID: 2157824 [TBL] [Abstract][Full Text] [Related]
19. Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21. van der Kooi AJ; van Meegen M; Ledderhof TM; McNally EM; de Visser M; Bolhuis PA Am J Hum Genet; 1997 Apr; 60(4):891-5. PubMed ID: 9106535 [TBL] [Abstract][Full Text] [Related]
20. Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome. Thomas NS; Williams H; Elsas LJ; Hopkins LC; Sarfarazi M; Harper PS J Med Genet; 1986 Dec; 23(6):596-8. PubMed ID: 3100805 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]