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3. Oculopharyngeal muscular dystrophy (OPMD)--report and genetic studies of an Australian kindred. Teh BT; Sullivan AA; Farnebo F; Zander C; Li FY; Strachan N; Schalling M; Larsson C; Sandstrom P Clin Genet; 1997 Jan; 51(1):52-5. PubMed ID: 9084936 [TBL] [Abstract][Full Text] [Related]
4. Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13. Stajich JM; Gilchrist JM; Lennon F; Lee A; Yamaoka L; Helms B; Gaskell PC; Donald L; Roses AD; Vance JM; Pericak-Vance MA Ann Neurol; 1996 Nov; 40(5):801-4. PubMed ID: 8957024 [TBL] [Abstract][Full Text] [Related]
5. Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation. Stajich JM; Gilchrist JM; Lennon F; Lee A; Yamaoka L; Rosi B; Gaskell PC; Pritchard M; Donald L; Roses AD; Vance JM; Pericak-Vance MA Neuromuscul Disord; 1997 Oct; 7 Suppl 1():S75-81. PubMed ID: 9392021 [TBL] [Abstract][Full Text] [Related]
6. Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy gene. Brais B; Bouchard JP; Gosselin F; Xie YG; Fardeau M; Tomé FM; Rouleau GA Neuromuscul Disord; 1997 Oct; 7 Suppl 1():S70-4. PubMed ID: 9392020 [TBL] [Abstract][Full Text] [Related]
8. Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the disease. Blumen SC; Brais B; Korczyn AD; Medinsky S; Chapman J; Asherov A; Nisipeanu P; Codère F; Bouchard JP; Fardeau M; Tomé FM; Rouleau GA Ann Neurol; 1999 Jul; 46(1):115-8. PubMed ID: 10401788 [TBL] [Abstract][Full Text] [Related]
9. Report on the first international symposium on oculopharyngeal muscular dystrophy. Neuromuscul Disord; 1997 Oct; 7 Suppl 1():S2-4. PubMed ID: 9392007 [No Abstract] [Full Text] [Related]
13. [A Japanese pedigree with oculopharyngeal muscular dystrophy]. Nohira O; Imai N; Okabe T; Hamaguchi K Rinsho Shinkeigaku; 1994 May; 34(5):461-5. PubMed ID: 7924058 [TBL] [Abstract][Full Text] [Related]
14. Oculopharyngeal muscular dystrophy as a cause of dysphagia in the elderly. Kiel DP J Am Geriatr Soc; 1986 Feb; 34(2):144-7. PubMed ID: 3944405 [TBL] [Abstract][Full Text] [Related]
15. Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families. Speer MC; Vance JM; Lennon-Graham F; Stajich JM; Viles KD; Gilchrist JM; Nigro V; McMichael R; Chutkow JG; Bartoloni L; Horrigan SK; Westbrook CA; Pericak-Vance MA Hum Hered; 1998; 48(4):179-84. PubMed ID: 9694248 [TBL] [Abstract][Full Text] [Related]
16. [Some questions and comments for the original article entitled "autosomal recessive oculopharyngeal 'muscular dystrophy'"]. Uyama E Rinsho Shinkeigaku; 1992 Jan; 32(1):94-5. PubMed ID: 1628446 [No Abstract] [Full Text] [Related]