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33. [Genetic counseling in myotonia and muscular dystrophy]. Becker PE Internist (Berl); 1978 Aug; 19(8):475-81. PubMed ID: 357337 [No Abstract] [Full Text] [Related]
34. The many faces of neurofibromatosis. Moore BC; Luce J Ariz Med; 1982 Feb; 39(2):99-102. PubMed ID: 6803740 [No Abstract] [Full Text] [Related]
35. Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature. Pascual-Castroviejo I; Gutierrez M; Morales C; Gonzalez-Mediero I; Martínez-Bermejo A; Pascual-Pascual SI Neuropediatrics; 1994 Aug; 25(4):183-90. PubMed ID: 7824090 [TBL] [Abstract][Full Text] [Related]
37. Electromyographic characteristics of congenital and early onset motor unit diseases. Fowler WM; Taylor RG; Munsat TL Arch Phys Med Rehabil; 1971 Aug; 52(8):343-61. PubMed ID: 5284447 [No Abstract] [Full Text] [Related]
38. Clinical consequences of heterozygosity for autosomal-recessive diseases. Vogel F Clin Genet; 1984 May; 25(5):381-415. PubMed ID: 6373070 [TBL] [Abstract][Full Text] [Related]
39. [Genetics and medicine]. Efroimson VP Klin Med (Mosk); 1974 Jun; 52(6):11-8. PubMed ID: 4608120 [No Abstract] [Full Text] [Related]