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46. Estimation of prognosis and prevalence of retinitis pigmentosa and Usher syndrome in Norway. Grøndahl J Clin Genet; 1987 Apr; 31(4):255-64. PubMed ID: 3594933 [TBL] [Abstract][Full Text] [Related]
47. Inverse retinitis pigmentosa, deafness, and hypogenitalism. Reinstein NM; Chalfin AI Am J Ophthalmol; 1971 Aug; 72(2):332-41. PubMed ID: 5571218 [No Abstract] [Full Text] [Related]
48. 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]
49. [On information regarding the Usher syndrome, a speial form of recessive damage to the labyrinth (a contribution on audiometric diagnosis)]. WAGEMANN W HNO; 1961 Mar; 9():151-3. PubMed ID: 13782438 [No Abstract] [Full Text] [Related]
51. Autosomal recessive cerebellar hypoplasia and tapeto-retinal degeneration: a new syndrome. Dooley JM; LaRoche GR; Tremblay F; Riding M Pediatr Neurol; 1992; 8(3):232-4. PubMed ID: 1622524 [TBL] [Abstract][Full Text] [Related]
52. Usher syndrome in four Norwegian counties. Grøndahl J; Mjøen S Clin Genet; 1986 Jul; 30(1):14-28. PubMed ID: 3757293 [TBL] [Abstract][Full Text] [Related]
53. Exclusion of Usher syndrome gene from much of chromosome 4. Smith RJ; Holcomb JD; Daiger SP; Caskey CT; Pelias MZ; Alford BR; Fontenot DD; Hejtmancik JF Cytogenet Cell Genet; 1989; 50(2-3):102-6. PubMed ID: 2776474 [TBL] [Abstract][Full Text] [Related]
54. Distinctive audiometric features between USH2A and USH2B subtypes of Usher syndrome. Hmani-Aifa M; Ben Arab S; Kharrat K; Orten DJ; Boulila-Elgaied A; Drira M; Hachicha S; Kimberling WJ; Ayadi H J Med Genet; 2002 Apr; 39(4):281-3. PubMed ID: 11950859 [No Abstract] [Full Text] [Related]
55. Clinical heterogeneity in a family with mutations in USH2A. Lenassi E; Robson AG; Luxon LM; Bitner-Glindzicz M; Webster AR JAMA Ophthalmol; 2015 Mar; 133(3):352-5. PubMed ID: 25521520 [No Abstract] [Full Text] [Related]
56. Usher syndrome: correlation between visual field size and maximal ERG response b-wave amplitude. Iannaccone A Adv Exp Med Biol; 2003; 533():123-31. PubMed ID: 15180256 [No Abstract] [Full Text] [Related]
57. [A new autosomal-recessive hereditary syndrome. Multiple peripheral pulmonary stenosis, brachytelephalangia, inner-ear deafness, ossification or calcification of cartilages]. Keutel J; Jörgensen G; Gabriel P Dtsch Med Wochenschr; 1971 Oct; 96(43):1676-81 passim. PubMed ID: 5099199 [No Abstract] [Full Text] [Related]