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25. Naevoid basal cell carcinoma syndrome and Charcot-Marie-Tooth disease: two autosomal dominant disorders segregating in a family. Heimler A, Friedman E, Rosenthal AD. J Med Genet; 1978 Aug; 15(4):288-91. PubMed ID: 712760 [Abstract] [Full Text] [Related]
26. Heterogeneity evidence and linkage studies on Charcot-Marie-Tooth disease. Griffiths LR, Zwi MB, McLeod JG, Ross DA, Nicholson GA. Neurology; 1989 Feb; 39(2 Pt 1):280-1. PubMed ID: 2915802 [Abstract] [Full Text] [Related]
27. Peroneal musclar atrophy (of Charcot-Marie-Tooth) in two African brothers. Billinghurst JR. Afr J Med Med Sci; 1976 Dec; 5(4):269-72. PubMed ID: 829740 [Abstract] [Full Text] [Related]
28. X-linked Charcot-Marie-Tooth disease. A linkage study in a large family by using 12 probes of the pericentromeric region. Mostacciuolo ML, Müller E, Fardin P, Micaglio GF, Bardoni B, Guioli S, Camerino G, Danieli GA. Hum Genet; 1991 May; 87(1):23-7. PubMed ID: 1674715 [Abstract] [Full Text] [Related]
30. Recessive inheritance in a neuronal motor neuropathy form of peroneal muscular atrophy. Frajman M, Brilla E, Gutiérrez A, Hun L. Rev Invest Clin; 1983 May; 35(4):305-8. PubMed ID: 6672928 [No Abstract] [Full Text] [Related]
35. Genetic aspects of hereditary motor and sensory neuropathy (types I and II). Harding AE, Thomas PK. J Med Genet; 1980 Oct; 17(5):329-36. PubMed ID: 7218272 [Abstract] [Full Text] [Related]