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Journal Abstract Search

240 related items for PubMed ID: 9765703

  • 21. Innovative approach to genetic counseling services for the deaf population.
    Arnos KS, Cunningham M, Israel J, Marazita ML.
    Am J Med Genet; 1992 Oct 01; 44(3):345-51. PubMed ID: 1488983
    [Abstract] [Full Text] [Related]

  • 22. Consanguinity and deafness in Omani children.
    Khabori MA, Patton MA.
    Int J Audiol; 2008 Jan 01; 47(1):30-3. PubMed ID: 18196484
    [Abstract] [Full Text] [Related]

  • 23. 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 Jan 01; 15(3):59-64. PubMed ID: 14727345
    [Abstract] [Full Text] [Related]

  • 24. Genetic testing and genetic counseling for deafness: the future is here.
    Brunger JW, Matthews AL, Smith RH, Robin NH.
    Laryngoscope; 2001 Apr 01; 111(4 Pt 1):715-8. PubMed ID: 11359145
    [Abstract] [Full Text] [Related]

  • 25. Genetic heterogeneity study of non-syndromic autosomal recessive sensorineural deafness within the Tunisian population.
    Chaabani H, Ben Arab S, Chebbi K.
    Ann Genet; 1995 Apr 01; 38(3):158-61. PubMed ID: 8540687
    [Abstract] [Full Text] [Related]

  • 26. Cochlear implants in deaf children.
    Al-Shaikh AH, Zakzouk SM, Metwalli AA, Dasugi AA.
    Saudi Med J; 2002 Apr 01; 23(4):441-4. PubMed ID: 11953772
    [Abstract] [Full Text] [Related]

  • 27. [Diagnosing hearing impairment in children].
    Hempel JM.
    MMW Fortschr Med; 2006 May 11; 148(19):26-8, 30. PubMed ID: 16736701
    [Abstract] [Full Text] [Related]

  • 28. Etiology of deafness in Afyon school for the deaf in Turkey.
    Dereköy FS.
    Int J Pediatr Otorhinolaryngol; 2000 Sep 29; 55(2):125-31. PubMed ID: 11006452
    [Abstract] [Full Text] [Related]

  • 29. Causes of childhood deafness in Pukhtoonkhwa Province of Pakistan and the role of consanguinity.
    Sajjad M, Khattak AA, Bunn JE, Mackenzie I.
    J Laryngol Otol; 2008 Oct 29; 122(10):1057-63. PubMed ID: 18423085
    [Abstract] [Full Text] [Related]

  • 30. Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome).
    Desir J, Abramowicz M.
    Orphanet J Rare Dis; 2008 Oct 15; 3():28. PubMed ID: 18922146
    [Abstract] [Full Text] [Related]

  • 31. Comprehensive survey of mutations in RP2 and RPGR in patients affected with distinct retinal dystrophies: genotype-phenotype correlations and impact on genetic counseling.
    Pelletier V, Jambou M, Delphin N, Zinovieva E, Stum M, Gigarel N, Dollfus H, Hamel C, Toutain A, Dufier JL, Roche O, Munnich A, Bonnefont JP, Kaplan J, Rozet JM.
    Hum Mutat; 2007 Jan 15; 28(1):81-91. PubMed ID: 16969763
    [Abstract] [Full Text] [Related]

  • 32. [Acute sensorineural hearing loss at the Otorhinolaryngology Department of the General Hospital in Subotica 1991-1996].
    Rakić N.
    Med Pregl; 1999 Jan 15; 52(1-2):44-52. PubMed ID: 10352504
    [Abstract] [Full Text] [Related]

  • 33. 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 15; 72(2):249-55. PubMed ID: 18022253
    [Abstract] [Full Text] [Related]

  • 34. [Hereditary hearing loss: genetic counselling].
    Cabanillas Farpón R, Cadiñanos Bañales J.
    Acta Otorrinolaringol Esp; 2012 Feb 15; 63(3):218-29. PubMed ID: 21514544
    [Abstract] [Full Text] [Related]

  • 35. Incidence of auditory neuropathy among the deaf school students.
    Duman K, Ayçiçek A, Sargin R, Kenar F, Yilmaz MD, Dereköy FS.
    Int J Pediatr Otorhinolaryngol; 2008 Jul 15; 72(7):1091-5. PubMed ID: 18486242
    [Abstract] [Full Text] [Related]

  • 36. Speech perception in congenitally, pre-lingually and post-lingually deaf children expressed in an equivalent hearing loss value.
    Rotteveel LJ, Snik AF, Vermeulen AM, Cremers CW, Mylanus EA.
    Clin Otolaryngol; 2008 Dec 15; 33(6):560-9. PubMed ID: 19126130
    [Abstract] [Full Text] [Related]

  • 37. [Factors causing deafness in deaf-mute students].
    Zhuang J.
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 1989 Dec 15; 24(4):204-6, 253-4. PubMed ID: 2486072
    [Abstract] [Full Text] [Related]

  • 38. The Perrault syndrome: clinical report and review.
    Nishi Y, Hamamoto K, Kajiyama M, Kawamura I.
    Am J Med Genet; 1988 Nov 15; 31(3):623-9. PubMed ID: 3067578
    [Abstract] [Full Text] [Related]

  • 39. [Differential approach to genetic prognosis for progeny in cases of sporadic sensorineural deafness in children].
    Bliumina MG, Moskovkina AG.
    Vestn Otorinolaringol; 1983 Nov 15; (1):29-32. PubMed ID: 6829114
    [No Abstract] [Full Text] [Related]

  • 40. Profound and total deafness in Owerri, Nigeria.
    Chukuezi AB.
    East Afr Med J; 1991 Nov 15; 68(11):905-12. PubMed ID: 1800085
    [Abstract] [Full Text] [Related]

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