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Journal Abstract Search

185 related items for PubMed ID: 1090886

  • 1. Symposium on sensorineural hearing loss in children: early detection and intervention. Genetic factors in deafness of early life.
    Nance WE, Sweeney A.
    Otolaryngol Clin North Am; 1975 Feb; 8(1):19-48. PubMed ID: 1090886
    [Abstract] [Full Text] [Related]

  • 2. Symposium on sensorineural hearing loss in children: early detection and intervention. Histopathology of sensorineural hearing loss in children.
    Altenau MM.
    Otolaryngol Clin North Am; 1975 Feb; 8(1):49-58. PubMed ID: 1118165
    [Abstract] [Full Text] [Related]

  • 3. Genetic approaches to the nosology of deafness.
    Fraser GR.
    Birth Defects Orig Artic Ser; 1971 Mar; 07(4):52-63. PubMed ID: 4950942
    [Abstract] [Full Text] [Related]

  • 4. [Forms of monosymptomatic hereditary sensorineural hearing loss and deafness in the Leipzig area].
    Oeken J, König E.
    HNO; 1993 Jun; 41(6):301-10. PubMed ID: 8365917
    [Abstract] [Full Text] [Related]

  • 5. Incidence of genetic factors in the causation of deafness in childhood.
    Lenzi A, Zaghis A.
    Scand Audiol Suppl; 1988 Jun; 30():37-41. PubMed ID: 3147507
    [Abstract] [Full Text] [Related]

  • 6. Genetic aspects of the BOR syndrome--branchial fistulas, ear pits, hearing loss, and renal anomalies.
    Fraser FC, Ling D, Clogg D, Nogrady B.
    Am J Med Genet; 1978 Jun; 2(3):241-52. PubMed ID: 263442
    [Abstract] [Full Text] [Related]

  • 7. [Hereditary unilateral deaf-mutism as a variable manifestation of bilateral deaf-mutism or hearing loss].
    Graf K.
    Laryngorhinootologie; 1992 May; 71(5):242-5. PubMed ID: 1616543
    [Abstract] [Full Text] [Related]

  • 8. [Genetic study of sensorineural hearing loss].
    Bliumina MG, Moskovkina AG.
    Genetika; 1982 May; 18(6):1012-7. PubMed ID: 7201942
    [Abstract] [Full Text] [Related]

  • 9. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 10. Genetic causes of hearing loss in children.
    Cantani A.
    Padiatr Padol; 1989 Aug; 24(4):321-30. PubMed ID: 2694074
    [Abstract] [Full Text] [Related]

  • 11. [Genetic counseling in Waardenburg's syndrome].
    Hageman MJ.
    Ned Tijdschr Geneeskd; 1979 Nov 10; 123(45):1929-32. PubMed ID: 514381
    [No Abstract] [Full Text] [Related]

  • 12. Symposium on sensorineural hearing loss in children: early detection and intervention. Evaluation of the child with sensorineural hearing impairment.
    Linthicum FH.
    Otolaryngol Clin North Am; 1975 Feb 10; 8(1):69-75. PubMed ID: 1167956
    [Abstract] [Full Text] [Related]

  • 13. [Prenatal causes of sensorineural hearing loss in children (author's transl)].
    Jahnke V.
    Laryngol Rhinol Otol (Stuttg); 1979 Nov 10; 58(11):811-6. PubMed ID: 231158
    [Abstract] [Full Text] [Related]

  • 14. Phenotypic characterization of hereditary hearing impairment linked to DFNA25.
    Thirlwall AS, Brown DJ, McMillan PM, Barker SE, Lesperance MM.
    Arch Otolaryngol Head Neck Surg; 2003 Aug 10; 129(8):830-5. PubMed ID: 12925340
    [Abstract] [Full Text] [Related]

  • 15. Usher syndrome in four hard-of-hearing siblings.
    Davenport SL, O'Nuallain S, Omenn GS, Wilkus RJ.
    Pediatrics; 1978 Oct 10; 62(4):578-83. PubMed ID: 714590
    [Abstract] [Full Text] [Related]

  • 16. Schizophrenia and mental retardation associated in a pedigree with retinitis pigmentosa and sensorineural deafness.
    Sharp CW, Muir WJ, Blackwood DH, Walker M, Gosden C, St Clair DM.
    Am J Med Genet; 1994 Dec 15; 54(4):354-60. PubMed ID: 7726208
    [Abstract] [Full Text] [Related]

  • 17. Renal prognosis in Alport's and related syndromes: influence of the mode of inheritance.
    Pochet JM, Bobrie G, Landais P, Goldfarb B, Grünfeld JP.
    Nephrol Dial Transplant; 1989 Dec 15; 4(12):1016-21. PubMed ID: 2517321
    [Abstract] [Full Text] [Related]

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