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22. Emery-Dreifuss syndrome: genetic and clinical varieties. Rudenskaya GE; Ginter EK; Petrin AN; Djomina NA Am J Med Genet; 1994 Apr; 50(3):228-33. PubMed ID: 8042665 [TBL] [Abstract][Full Text] [Related]
23. Intrafamilial variability in spinal muscular atrophy. Prot J; Sawicka E Pol Med J; 1969; 8(5):1165-9. PubMed ID: 5383931 [No Abstract] [Full Text] [Related]
24. [A case of myotubular myopathy with autosomal dominant inheritance (author's transl)]. Wakabayashi Y; Arimura Y; Sawaguchi Y; Koike H; Yoshino Y No To Shinkei; 1980 Jul; 32(7):715-22. PubMed ID: 7407023 [No Abstract] [Full Text] [Related]
25. [Benign familial proximal amyotrophy with late onset (presentation of a case with dominant hereditary transmission)]. Cianchetti C; Tonato M; Signorini E Riv Patol Nerv Ment; 1969 Dec; 90(6):481-92. PubMed ID: 5406113 [No Abstract] [Full Text] [Related]
26. A clinical and genetic study of chronic proximal spinal muscular atrophy. Bundey S; Lovelace RE Brain; 1975 Sep; 98(3):455-72. PubMed ID: 1182487 [TBL] [Abstract][Full Text] [Related]
27. The infantile proximal spinal muscular atrophies in Switzerland. Zellweger H; Hanhart E Helv Paediatr Acta; 1972 Sep; 27(4):355-60. PubMed ID: 4644272 [No Abstract] [Full Text] [Related]
28. [Clinical features of bulbar-spinal muscular atrophy (author's transl)]. Mukai E Rinsho Shinkeigaku; 1980 Apr; 20(4):255-63. PubMed ID: 7408329 [No Abstract] [Full Text] [Related]
29. Juvenile spinal muscular atrophy--a new hexosaminidase deficiency phenotype. Johnson WG; Wigger HJ; Karp HR; Glaubiger LM; Rowland LP Trans Am Neurol Assoc; 1981; 106():215-8. PubMed ID: 7348998 [No Abstract] [Full Text] [Related]
31. [A case of scapuloperoneal muscular atrophy with contracture of joints and cardiopathy (author's transl)]. Kuriyama M; Ouchi M; Umezaki H; Sants T Rinsho Shinkeigaku; 1977 Sep; 17(9):575-81. PubMed ID: 144575 [No Abstract] [Full Text] [Related]