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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

134 related items for PubMed ID: 18005182

  • 1. Sex-linked deafness.
    Petersen MB, Wang Q, Willems PJ.
    Clin Genet; 2008 Jan; 73(1):14-23. PubMed ID: 18005182
    [Abstract] [Full Text] [Related]

  • 2. Mitochondrial deafness.
    Kokotas H, Petersen MB, Willems PJ.
    Clin Genet; 2007 May; 71(5):379-91. PubMed ID: 17489842
    [Abstract] [Full Text] [Related]

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

  • 4. Linkage and association studies in a Malaysian family with autosomal recessive non-syndromic hearing loss.
    Farah WI, Aminuddin BS, Ruszymah BH.
    Malays J Pathol; 2006 Jun; 28(1):23-33. PubMed ID: 17694956
    [Abstract] [Full Text] [Related]

  • 5. [Infrequent X chromosome abnormality and X-linked syndromic deafness].
    Wang YJ, Shi XL, Nie JW, Ni B, Yin ZC, Dai HP.
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2004 Oct; 29(5):500-3. PubMed ID: 16137031
    [Abstract] [Full Text] [Related]

  • 6. A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families.
    Alasti F, Sanati MH, Behrouzifard AH, Sadeghi A, de Brouwer AP, Kremer H, Smith RJ, Van Camp G.
    Int J Pediatr Otorhinolaryngol; 2008 Feb; 72(2):249-55. PubMed ID: 18022253
    [Abstract] [Full Text] [Related]

  • 7. Syndromic choroideremia: sublocalization of phenotypes associated with Martin-Probst deafness mental retardation syndrome.
    Poloschek CM, Kloeckener-Gruissem B, Hansen LL, Bach M, Berger W.
    Invest Ophthalmol Vis Sci; 2008 Sep; 49(9):4096-104. PubMed ID: 18487380
    [Abstract] [Full Text] [Related]

  • 8. [Non-syndromic familial deafness. Review and genetic study].
    Guiral H, Flores JC, Risco J, Figuerola E, Pellicer F.
    Acta Otorrinolaringol Esp; 1996 Sep; 47(4):272-6. PubMed ID: 8962727
    [Abstract] [Full Text] [Related]

  • 9. Genetics of aminoglycoside-induced and prelingual non-syndromic mitochondrial hearing impairment: a review.
    Bindu LH, Reddy PP.
    Int J Audiol; 2008 Nov; 47(11):702-7. PubMed ID: 19031229
    [Abstract] [Full Text] [Related]

  • 10. An overview of hereditary hearing loss.
    Bayazit YA, Yilmaz M.
    ORL J Otorhinolaryngol Relat Spec; 2006 Nov; 68(2):57-63. PubMed ID: 16428895
    [Abstract] [Full Text] [Related]

  • 11. [Hereditary hearing loss: new diagnostic possibilities].
    Hergersberg M, Weigell-Weber M.
    Schweiz Med Wochenschr; 2000 Apr 01; 130(13):485-9. PubMed ID: 10812644
    [Abstract] [Full Text] [Related]

  • 12. [Advance in molecular genetic research on X-linked syndromic hearing impairment].
    Huang M, Zhang D.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec 10; 34(6):928-933. PubMed ID: 29188633
    [Abstract] [Full Text] [Related]

  • 13. Audiologic features of the X-linked progressive mixed deafness syndrome with perilymphatic gusher during stapes gusher.
    Cremers CW.
    Am J Otol; 1985 May 10; 6(3):243-6. PubMed ID: 4039896
    [Abstract] [Full Text] [Related]

  • 14. A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21.
    Lezirovitz K, Braga MC, Thiele-Aguiar RS, Auricchio MT, Pearson PL, Otto PA, Mingroni-Netto RC.
    Clin Genet; 2009 May 10; 75(5):490-3. PubMed ID: 19159392
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  • 20. A mutational analysis of the SLC26A4 gene in Spanish hearing-impaired families provides new insights into the genetic causes of Pendred syndrome and DFNB4 hearing loss.
    Pera A, Villamar M, Viñuela A, Gandía M, Medà C, Moreno F, Hernández-Chico C.
    Eur J Hum Genet; 2008 Aug 10; 16(8):888-96. PubMed ID: 18285825
    [Abstract] [Full Text] [Related]

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