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4. [An unusual picture of pigmentary dermatologic disease associated with retinitis pigmentosa, cataract and congenital deafness, oligophrenia and cerebellar ataxia]. Scialdone D; Artifoni E G Ital Oftalmol; 1964; 17(1):49-60. PubMed ID: 5827882 [No Abstract] [Full Text] [Related]
5. Reduced incidence of congenital and prelingual deafness. Marcus RE Arch Otolaryngol; 1970 Oct; 92(4):343-7. PubMed ID: 5455575 [No Abstract] [Full Text] [Related]
6. Sensorineural deafness: familial incidence and additional defects--study of a school for deaf children. Fishman JE; Cristal N Am J Med Sci; 1973 Aug; 266(2):111-7. PubMed ID: 4542658 [No Abstract] [Full Text] [Related]
7. [Cardio-cutaneous syndromes of genetic origin]. Pernot C; Worms AM; Henry M Nouv Presse Med; 1973 Oct; 2(36):2395-400. PubMed ID: 4201000 [No Abstract] [Full Text] [Related]
8. PROFOUND CHILDHOOD DEAFNESS. FRASER GR J Med Genet; 1964 Dec; 1(2):118-51. PubMed ID: 14234108 [No Abstract] [Full Text] [Related]
10. [Hallgren's syndrome in one family: retinitis pigmentosa, congenital deafness and ataxia]. Urquidi GA; Topaz AM Acta Neurol Latinoam; 1979; 25(1-2):75-9. PubMed ID: 583386 [TBL] [Abstract][Full Text] [Related]
11. Epidemiological and genetic studies of congenital profound deafness in the general population of Sichuan, China. Liu X; Xu L; Zhang S; Xu Y Am J Med Genet; 1994 Nov; 53(2):192-5. PubMed ID: 7856647 [TBL] [Abstract][Full Text] [Related]
12. Childhood deafness in Cape Town. Sellars S; Napier E; Beighton P S Afr Med J; 1975 Jul; 49(28):1135-8. PubMed ID: 1154167 [TBL] [Abstract][Full Text] [Related]
13. A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variation. Liu XZ; Hope C; Liang CY; Zou JM; Xu LR; Cole T; Mueller RF; Bundey S; Nance W; Steel KP; Brown SD Am J Hum Genet; 1999 Apr; 64(4):1221-5. PubMed ID: 10090909 [No Abstract] [Full Text] [Related]