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

PUBMED FOR HANDHELDS

Journal Abstract Search

241 related items for PubMed ID: 7468659

  • 41. [Clinical symptoms of branchio-oto-renal syndrome in a family with a positive test for EYA1 gene].
    Markova TG.
    Vestn Otorinolaringol; 2006; (6):25-8. PubMed ID: 17419499
    [Abstract] [Full Text] [Related]

  • 42.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 43.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 45. BOR and BO syndromes are allelic defects of EYA1.
    Vincent C, Kalatzis V, Abdelhak S, Chaib H, Compain S, Helias J, Vaneecloo FM, Petit C.
    Eur J Hum Genet; 1997 Aug; 5(4):242-6. PubMed ID: 9359046
    [Abstract] [Full Text] [Related]

  • 46. Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormalties.
    Colville D, Wang YY, Jamieson R, Collins F, Hood J, Savige J.
    Ophthalmic Genet; 2000 Dec; 21(4):217-25. PubMed ID: 11135492
    [Abstract] [Full Text] [Related]

  • 47. Eya1 expression in the developing ear and kidney: towards the understanding of the pathogenesis of Branchio-Oto-Renal (BOR) syndrome.
    Kalatzis V, Sahly I, El-Amraoui A, Petit C.
    Dev Dyn; 1998 Dec; 213(4):486-99. PubMed ID: 9853969
    [Abstract] [Full Text] [Related]

  • 48.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 49. Evidence for autosomal recessive inheritance of the syndrome of renal tubular acidosis with deafness.
    Nance WE, Sweeney A.
    Birth Defects Orig Artic Ser; 1971 Mar; 07(4):70-2. PubMed ID: 5173352
    [Abstract] [Full Text] [Related]

  • 50. 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; 129(8):830-5. PubMed ID: 12925340
    [Abstract] [Full Text] [Related]

  • 51. Quiz page April 2008: deafness, preauricular pits, and renal failure. BOR syndrome or Melnick-Fraser syndrome.
    Zar T, Aglieco F, Ranga KV.
    Am J Kidney Dis; 2008 Apr; 51(4):A44-6. PubMed ID: 18371523
    [No Abstract] [Full Text] [Related]

  • 52. Anatomical Changes and Audiological Profile in Branchio-oto-renal Syndrome: A Literature Review.
    Lindau TA, Cardoso AC, Rossi NF, Giacheti CM.
    Int Arch Otorhinolaryngol; 2014 Jan; 18(1):68-76. PubMed ID: 25992067
    [Abstract] [Full Text] [Related]

  • 53. Hemifacial microsomia and the branchio-oto-renal syndrome.
    Rollnick BR, Kaye CI.
    J Craniofac Genet Dev Biol Suppl; 1985 Jan; 1():287-95. PubMed ID: 3877103
    [Abstract] [Full Text] [Related]

  • 54. Branchio-oto-renal syndrome.
    Millman B, Gibson WS, Foster WP.
    Arch Otolaryngol Head Neck Surg; 1995 Aug; 121(8):922-5. PubMed ID: 7619422
    [Abstract] [Full Text] [Related]

  • 55. [Families with recurrent cases of Waardenburg-Klein syndrome].
    Bliumina MG, Moskovkina AG.
    Genetika; 1985 Jun; 21(6):1062-5. PubMed ID: 4029612
    [Abstract] [Full Text] [Related]

  • 56. Shoulder abnormalities in association with branchio-oto-renal dysplasia in a patient who also has familial joint laxity.
    Pennie BH, Marres HA.
    Int J Pediatr Otorhinolaryngol; 1992 May; 23(3):269-73. PubMed ID: 1592563
    [Abstract] [Full Text] [Related]

  • 57. Dominantly inherited renal adysplasia.
    McPherson E, Carey J, Kramer A, Hall JG, Pauli RM, Schimke RN, Tasin MH.
    Am J Med Genet; 1987 Apr; 26(4):863-72. PubMed ID: 3591828
    [Abstract] [Full Text] [Related]

  • 58. Autosomal dominant branchio-oto-renal syndrome--localization of a disease gene to chromosome 8q by linkage in a Dutch family.
    Kumar S, Kimberling WJ, Kenyon JB, Smith RJ, Marres HA, Cremers CW.
    Hum Mol Genet; 1992 Oct; 1(7):491-5. PubMed ID: 1307249
    [Abstract] [Full Text] [Related]

  • 59. Mitral valve prolapse as a new finding in branchio-oto-renal syndrome.
    Ayçiçek A, Sağlam H, Koçoğullari CU, Haktanir NT, Dereköy FS, Solak M.
    Clin Dysmorphol; 2010 Oct; 19(4):181-184. PubMed ID: 20845527
    [Abstract] [Full Text] [Related]

  • 60. Study of the etiology of deafness in an institutionalized population in Colombia.
    Tamayo ML, Bernal JE, Tamayo GE, Frias JL.
    Am J Med Genet; 1992 Nov 01; 44(4):405-8. PubMed ID: 1442876
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 13.