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Journal Abstract Search

101 related items for PubMed ID: 1928264

  • 1. Ultrastructural study of Norrie's disease.
    Van Nouhuys CE.
    Am J Ophthalmol; 1991 Oct 15; 112(4):475-7. PubMed ID: 1928264
    [No Abstract] [Full Text] [Related]

  • 2. Probably Norrie's disease due to mutation. Two sporadic sibships of two males each, a necropsy of one case, and, given Norrie's disease, a calculation of the gene mutation frequency.
    Phillips CI, Newton M, Duvall J, Holloway S, Levy AM.
    Br J Ophthalmol; 1986 Apr 15; 70(4):305-13. PubMed ID: 3964631
    [Abstract] [Full Text] [Related]

  • 3. [Norrie's disease].
    Vérin P, Comte P.
    Bull Soc Ophtalmol Fr; 1986 Apr 15; 86(8-9):1103-5. PubMed ID: 3568256
    [No Abstract] [Full Text] [Related]

  • 4. The molecular biology of Norrie's disease.
    Black G, Redmond RM.
    Eye (Lond); 1994 Apr 15; 8 ( Pt 5)():491-6. PubMed ID: 7835440
    [Abstract] [Full Text] [Related]

  • 5. Norrie's disease: close linkage with genetic markers from the proximal short arm of the X chromosome.
    Gal A, Stolzenberger C, Wienker T, Wieacker P, Ropers HH, Friedrich U, Bleeker-Wagemakers L, Pearson P, Warburg M.
    Clin Genet; 1985 Mar 15; 27(3):282-3. PubMed ID: 3857130
    [No Abstract] [Full Text] [Related]

  • 6. Falciform fold, retinal detachment, and Norrie's disease.
    Jacklin HN.
    Am J Ophthalmol; 1980 Jul 15; 90(1):76-80. PubMed ID: 7395960
    [Abstract] [Full Text] [Related]

  • 7. Ultrastructural study of Norrie's disease.
    Enyedi LB, de Juan E, Gaitan A.
    Am J Ophthalmol; 1991 Apr 15; 111(4):439-45. PubMed ID: 1781818
    [Abstract] [Full Text] [Related]

  • 8. Electrophysiological study of Norrie's disease. An X-linked recessive trait with hearing loss.
    Parving A, Elberling C, Warburg M.
    Audiology; 1978 Apr 15; 17(4):293-8. PubMed ID: 567472
    [Abstract] [Full Text] [Related]

  • 9. Norrie's disease.
    Johnston SS, Hanna JE, Nevin NC, Bryars JH.
    Birth Defects Orig Artic Ser; 1982 Apr 15; 18(6):729-38. PubMed ID: 6890861
    [No Abstract] [Full Text] [Related]

  • 10. Manifesting heterozygosity in Norrie's disease?
    Woodruff G, Newbury-Ecob R, Plaha DS, Young ID.
    Br J Ophthalmol; 1993 Dec 15; 77(12):813-4. PubMed ID: 8110678
    [No Abstract] [Full Text] [Related]

  • 11. Norrie's disease: a prospective study of development.
    Goodyear HM, Sonksen PM, McConachie H.
    Arch Dis Child; 1989 Nov 15; 64(11):1587-92. PubMed ID: 2604418
    [Abstract] [Full Text] [Related]

  • 12. [Norrie's disease].
    Brini A, Sacrez P, Levy JP.
    Ann Ocul (Paris); 1972 Jan 15; 205(1):1-16. PubMed ID: 4624828
    [No Abstract] [Full Text] [Related]

  • 13. Bilateral Norrie's disease in identical twins.
    Sukumaran K.
    Br J Ophthalmol; 1991 Mar 15; 75(3):179-80. PubMed ID: 2012789
    [Abstract] [Full Text] [Related]

  • 14. Norrie's disease--an x-linked syndrome of retinal malformation, mental retardation and deafness.
    Holmes LB.
    N Engl J Med; 1971 Feb 18; 284(7):367-8. PubMed ID: 4992907
    [No Abstract] [Full Text] [Related]

  • 15. The use of a DNA marker for carrier diagnosis in an X-linked disorder: Norrie's disease.
    Hill DF, Chapman CJ, Gardner RJ.
    N Z Med J; 1987 Mar 25; 100(820):166-8. PubMed ID: 3482910
    [Abstract] [Full Text] [Related]

  • 16. Norrie's disease in a French-Canadian kindred: attempt to detect carriers by DNA analysis.
    Polomeno RC, Zeesman S, MacDonald IM, Crozier DG, Tenniswood MP, Kaplan P.
    Can J Ophthalmol; 1987 Feb 25; 22(1):21-3. PubMed ID: 3815151
    [Abstract] [Full Text] [Related]

  • 17. Prenatal exclusion of Norrie's disease.
    Redmond RM, Graham CA, Kelly ED, Coleman M, Nevin NC.
    Br J Ophthalmol; 1992 Aug 25; 76(8):491-3. PubMed ID: 1390533
    [Abstract] [Full Text] [Related]

  • 18. Ocular histopathology of Norrie's disease.
    Apple DJ, Fishman GA, Goldberg MF.
    Am J Ophthalmol; 1974 Aug 25; 78(2):196-203. PubMed ID: 4211188
    [No Abstract] [Full Text] [Related]

  • 19. Audiometric tests in gene carriers of Norrie's disease.
    Parving A, Schwartz M.
    Int J Pediatr Otorhinolaryngol; 1991 Apr 25; 21(2):103-11. PubMed ID: 1679755
    [Abstract] [Full Text] [Related]

  • 20. Primary vitreoretinal dysplasia resembling Norrie's disease in a female: association with X autosome chromosomal translocation.
    Ohba N, Yamashita T.
    Br J Ophthalmol; 1986 Jan 25; 70(1):64-71. PubMed ID: 3947601
    [Abstract] [Full Text] [Related]

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