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Journal Abstract Search

215 related items for PubMed ID: 8962727

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

  • 2. [Etiological diagnosis of sensorineural deafness in children: a year-long review of genetic counseling for deaf people].
    Marlin S, Denoyelle F, Garabédian EN, Petit C.
    Ann Otolaryngol Chir Cervicofac; 1998 Feb; 115(1):3-8. PubMed ID: 9765703
    [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. Familial auditory neuropathy.
    Wang Q, Gu R, Han D, Yang W.
    Laryngoscope; 2003 Sep; 113(9):1623-9. PubMed ID: 12972945
    [Abstract] [Full Text] [Related]

  • 5. [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]

  • 6. Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature.
    Berrettini S, Forli F, Passetti S, Rocchi A, Pollina L, Cecchetti D, Mancuso M, Siciliano G.
    Biosci Rep; 2008 Feb; 28(1):49-59. PubMed ID: 18215147
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. 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]

  • 9. 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]

  • 10. Syndromic and non-syndromic deafness, molecular aspects of Pendred syndrome and its reported mutations.
    Shaukat S, Fatima Z, Zehra U, Waqar AB.
    J Ayub Med Coll Abbottabad; 2003 Feb; 15(3):59-64. PubMed ID: 14727345
    [Abstract] [Full Text] [Related]

  • 11. A review of genetic mutation in familial Hirschsprung's disease in South Africa: towards genetic counseling.
    Moore SW, Zaahl MG.
    J Pediatr Surg; 2008 Feb; 43(2):325-9. PubMed ID: 18280283
    [Abstract] [Full Text] [Related]

  • 12. 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]

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

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

  • 15. [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]

  • 16. Maternally inherited hearing impairment in a family with the mitochondrial DNA A7445G mutation.
    Hutchin TP, Lench NJ, Arbuzova S, Markham AF, Mueller RF.
    Eur J Hum Genet; 2001 Jan; 9(1):56-8. PubMed ID: 11175301
    [Abstract] [Full Text] [Related]

  • 17. Parental attitudes toward genetic testing for prelingual deafness in China.
    Fu S, Dong J, Wang C, Chen G.
    Int J Pediatr Otorhinolaryngol; 2010 Oct; 74(10):1122-5. PubMed ID: 20637511
    [Abstract] [Full Text] [Related]

  • 18. Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness.
    Ouyang XM, Xia XJ, Verpy E, Du LL, Pandya A, Petit C, Balkany T, Nance WE, Liu XZ.
    Hum Genet; 2002 Jul; 111(1):26-30. PubMed ID: 12136232
    [Abstract] [Full Text] [Related]

  • 19. [Family history, clinical features, and molecular characterization of a patient with autosomal recessive non-syndromic hearing loss].
    Düzcan F, Wollnik B, Tepeli E, Ardiç FN, Uyguner O, Bağci H.
    Kulak Burun Bogaz Ihtis Derg; 2003 Sep; 11(3):85-8. PubMed ID: 14699249
    [Abstract] [Full Text] [Related]

  • 20. The syndrome of anosmia with hypogonadotropic hypogonadism: a genetic study of 18 new families and a review.
    White BJ, Rogol AD, Brown KS, Lieblich JM, Rosen SW.
    Am J Med Genet; 1983 Jul; 15(3):417-35. PubMed ID: 6881209
    [Abstract] [Full Text] [Related]

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