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Journal Abstract Search

63 related items for PubMed ID: 6829114

  • 1. [Differential approach to genetic prognosis for progeny in cases of sporadic sensorineural deafness in children].
    Bliumina MG, Moskovkina AG.
    Vestn Otorinolaringol; 1983; (1):29-32. PubMed ID: 6829114
    [No 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. Nonsyndromic deafness.
    Nance WE.
    Birth Defects Orig Artic Ser; 1980 Feb; 16(7):35-46. PubMed ID: 7011439
    [No Abstract] [Full Text] [Related]

  • 4. [Mode of inheritance of congenital deaf-mutism].
    Hu DN, Qiu WQ, Wu BT, Fang LZ, Zhou F, Gu YP, Zhang QH, Yan JH.
    Yi Chuan Xue Bao; 1988 Feb; 15(4):303-8. PubMed ID: 3273676
    [No Abstract] [Full Text] [Related]

  • 5. Genetic counseling in congenital deafness.
    François J, De Bie SD, Matton-Van Leuven MT.
    Acta Genet Med Gemellol (Roma); 1975 Feb; 24(3-4):295-7. PubMed ID: 1235934
    [Abstract] [Full Text] [Related]

  • 6. Waardenburg syndrome in the Turkish deaf population.
    Silan F, Zafer C, Onder I.
    Genet Couns; 2006 Feb; 17(1):41-8. PubMed ID: 16719276
    [Abstract] [Full Text] [Related]

  • 7. [Clinical examinations in Usher's syndrome].
    Lubiński W, Palacz O, Zajaczek S.
    Klin Oczna; 1996 Jan; 98(1):55-8. PubMed ID: 9019578
    [Abstract] [Full Text] [Related]

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

  • 9. Genetic epidemiological studies of early-onset deafness in the U.S. school-age population.
    Marazita ML, Ploughman LM, Rawlings B, Remington E, Arnos KS, Nance WE.
    Am J Med Genet; 1993 Jun 15; 46(5):486-91. PubMed ID: 8322805
    [Abstract] [Full Text] [Related]

  • 10. Genetic heterogeneity study of non-syndromic autosomal recessive sensorineural deafness within the Tunisian population.
    Chaabani H, Ben Arab S, Chebbi K.
    Ann Genet; 1995 Jun 15; 38(3):158-61. PubMed ID: 8540687
    [Abstract] [Full Text] [Related]

  • 11. [Practical directives for the genetic counselor in cases of isolated hereditary deafness].
    de Bie S, Matton-van Leuven MT, François J.
    J Genet Hum; 1976 Nov 15; 24 Suppl():195-8. PubMed ID: 1025270
    [No Abstract] [Full Text] [Related]

  • 12. [Non-syndromic familial deafness. Review and genetic study].
    Guiral H, Flores JC, Risco J, Figuerola E, Pellicer F.
    Acta Otorrinolaringol Esp; 1996 Nov 15; 47(4):272-6. PubMed ID: 8962727
    [Abstract] [Full Text] [Related]

  • 13. [Genetic deafness and genetic counseling].
    Rolland M.
    Rev Laryngol Otol Rhinol (Bord); 1988 Nov 15; 109(4):357-60. PubMed ID: 3238203
    [No Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. [Genetic study of sensorineural hearing loss].
    Bliumina MG, Moskovkina AG.
    Genetika; 1982 Feb 03; 18(6):1012-7. PubMed ID: 7201942
    [Abstract] [Full Text] [Related]

  • 16. [Genetic counseling in profound deafness].
    Clarós P, Antich J, Clarós A, Clarós Doménech A.
    Acta Otorrinolaringol Esp; 1996 Feb 03; 47(3):169-74. PubMed ID: 8924278
    [Abstract] [Full Text] [Related]

  • 17. [Congenital and hereditary hearing disorders in population of the Nakhichevan Autonomous Republic].
    Panakhiian VM.
    Vestn Otorinolaringol; 2004 Feb 03; (6):22-4. PubMed ID: 15699983
    [Abstract] [Full Text] [Related]

  • 18. Phenotype and counseling in lacrimo-auriculo-dento-digital (LADD) syndrome.
    Horn D, Witkowski R.
    Genet Couns; 1993 Feb 03; 4(4):305-9. PubMed ID: 8110420
    [Abstract] [Full Text] [Related]

  • 19. [Genetic counseling in deafness].
    Boschetti R.
    Rev Prat; 1976 Feb 01; 26(7):527-32, 551-2, 555-9 passim. PubMed ID: 1265401
    [No Abstract] [Full Text] [Related]

  • 20. The otolaryngologist as genetic counselor.
    Jahn AF, Gardner HA.
    Otolaryngol Clin North Am; 1981 Feb 01; 14(1):251-6. PubMed ID: 7254844
    [No Abstract] [Full Text] [Related]

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