These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


103 related items for PubMed ID: 1679755

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

  • 2. 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]

  • 3. Norrie's disease: delineation of carriers among daughters of obligate carriers by linkage analysis.
    Warburg M, Friedrich U, Bleeker-Wagemakers L, Wienker TF, Gal A, Ropers HH.
    Trans Ophthalmol Soc U K (1962); 1986 Mar 25; 105 ( Pt 1)():88-93. PubMed ID: 3459299
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. 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 25; 70(4):305-13. PubMed ID: 3964631
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. 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]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Hearing assessment in children with stapedius reflex threshold measurements--an alternative objective approach.
    Jauhiainen T, Marttila TI, Karikoski J.
    Adv Otorhinolaryngol; 1997 Feb 25; 51():1-7. PubMed ID: 9017064
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Acoustic reflex relaxation in sensorineural hearing loss.
    Letien WC, Bess FH.
    Arch Otolaryngol; 1975 Oct 18; 101(10):617-21. PubMed ID: 1164227
    [Abstract] [Full Text] [Related]

  • 17. Autosomal recessive nonsyndromal profound childhood deafness in a large pedigree. Audiometric features of the affected persons and the obligate carriers.
    Marres HA, Cremers CW.
    Arch Otolaryngol Head Neck Surg; 1989 May 18; 115(5):591-5. PubMed ID: 2706105
    [Abstract] [Full Text] [Related]

  • 18. [Recruitment detection--a comparison of category loudness scaling and classical supra-threshold audiometry].
    Kiessling J, Pfreimer C, Schubert M.
    Laryngorhinootologie; 1996 Jan 18; 75(1):10-7. PubMed ID: 8851113
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 6.