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2. [Permanent familial auricular paralysis probably due to a genetic disease of the Charcot-Marie type]. Bensaid J, Gilgenkrantz JM, Fernandez F, Dodinot B, Scebat L, Himbert J, Faivre G, Lenegre J. Nouv Presse Med; 1972 Apr 01; 1(14):959. PubMed ID: 5019302 [No Abstract] [Full Text] [Related]
3. [Familial myocardial disease. On 2 clinical cases]. Cristodorescu R, Ardeleanu R, Drăgulescu I, Coreanu G. Med Interna (Bucur); 1971 Oct 01; 23(10):1229-38. PubMed ID: 5127133 [No Abstract] [Full Text] [Related]
4. [Significance of sibship studies--as demonstrated on a new family with neural muscular atrophy (Charcot-Marie-Tooth)]. Wagner A. Z Arztl Fortbild (Jena); 1972 Jun 15; 66(12):621-4. PubMed ID: 4538352 [No Abstract] [Full Text] [Related]