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Journal Abstract Search

97 related items for PubMed ID: 10051011

  • 1. Variations in genetic assessment and recurrence risks quoted for childhood deafness: a survey of clinical geneticists.
    Parker MJ, Fortnum H, Young ID, Davis AC.
    J Med Genet; 1999 Feb; 36(2):125-30. PubMed ID: 10051011
    [Abstract] [Full Text] [Related]

  • 2. Meeting the needs of parents around the time of diagnosis of disability among their children: evaluation of a novel program for information, support, and liaison by key workers.
    Rahi JS, Manaras I, Tuomainen H, Hundt GL.
    Pediatrics; 2004 Oct; 114(4):e477-82. PubMed ID: 15466074
    [Abstract] [Full Text] [Related]

  • 3. [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]

  • 4. Etiological diagnosis of bilateral, sensorineural hearing impairment in a pediatric Greek population.
    Riga M, Psarommatis I, Lyra Ch, Douniadakis D, Tsakanikos M, Neou P, Apostolopoulos N.
    Int J Pediatr Otorhinolaryngol; 2005 Apr; 69(4):449-55. PubMed ID: 15763280
    [Abstract] [Full Text] [Related]

  • 5. [Attitudes towards prenatal diagnosis of deafness among parents to children with cochlear implants].
    Thorsen A, Devantier L, Ovesen T.
    Ugeskr Laeger; 2009 Apr 20; 171(17):1387-91. PubMed ID: 19413935
    [Abstract] [Full Text] [Related]

  • 6. Parental attitudes toward genetic testing for prelingual deafness in China.
    Fu S, Dong J, Wang C, Chen G.
    Int J Pediatr Otorhinolaryngol; 2010 Oct 20; 74(10):1122-5. PubMed ID: 20637511
    [Abstract] [Full Text] [Related]

  • 7. American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility.
    American Society of Clinical Oncology.
    J Clin Oncol; 2003 Jun 15; 21(12):2397-406. PubMed ID: 12692171
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 122(10):1057-63. PubMed ID: 18423085
    [Abstract] [Full Text] [Related]

  • 9. Genetic testing and genetic counseling for deafness: the future is here.
    Brunger JW, Matthews AL, Smith RH, Robin NH.
    Laryngoscope; 2001 Apr 15; 111(4 Pt 1):715-8. PubMed ID: 11359145
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.
    Dai P, Liu X, Han D, Qian Y, Huang D, Yuan H, Li W, Yu F, Zhang R, Lin H, He Y, Yu Y, Sun Q, Qin H, Li R, Zhang X, Kang D, Cao J, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2006 Feb 03; 340(1):194-9. PubMed ID: 16375862
    [Abstract] [Full Text] [Related]

  • 12. [Societal cost of pre-lingual deafness].
    Bubbico L, Bartolucci MA, Broglio D, Boner A.
    Ann Ig; 2007 Feb 03; 19(2):143-52. PubMed ID: 17547219
    [Abstract] [Full Text] [Related]

  • 13. [Organization of medico-genetic counseling for hereditary hearing impairment].
    Markova TG.
    Vestn Otorinolaringol; 2009 Feb 03; (1):34-6. PubMed ID: 19365361
    [Abstract] [Full Text] [Related]

  • 14. Prevalence and age of identification of permanent childhood hearing impairment in Cyprus.
    Hadjikakou K, Bamford J.
    Audiology; 2000 Feb 03; 39(4):198-201. PubMed ID: 10963440
    [Abstract] [Full Text] [Related]

  • 15. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 03; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 16. Parents' preferences for services for children with hearing loss: a conjoint analysis study.
    Fitzpatrick E, Coyle DE, Durieux-Smith A, Graham ID, Angus DE, Gaboury I.
    Ear Hear; 2007 Dec 03; 28(6):842-9. PubMed ID: 17982370
    [Abstract] [Full Text] [Related]

  • 17. Cochlear implants in deaf children.
    Al-Shaikh AH, Zakzouk SM, Metwalli AA, Dasugi AA.
    Saudi Med J; 2002 Apr 03; 23(4):441-4. PubMed ID: 11953772
    [Abstract] [Full Text] [Related]

  • 18. A refined symptom-based approach to diagnose pulmonary tuberculosis in children.
    Marais BJ, Gie RP, Hesseling AC, Schaaf HS, Lombard C, Enarson DA, Beyers N.
    Pediatrics; 2006 Nov 03; 118(5):e1350-9. PubMed ID: 17079536
    [Abstract] [Full Text] [Related]

  • 19. Consanguinity and deafness in Omani children.
    Khabori MA, Patton MA.
    Int J Audiol; 2008 Jan 03; 47(1):30-3. PubMed ID: 18196484
    [Abstract] [Full Text] [Related]

  • 20. [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]

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