These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 17828104)

  • 1. [Progress in genetic testing and prevention of hereditary hearing disorders].
    Markova TG; Poliakov AV
    Vestn Otorinolaringol; 2007; (4):7-10. PubMed ID: 17828104
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary sensorineural hearing loss: advances in molecular genetics and mutation analysis.
    Schrijver I; Gardner P
    Expert Rev Mol Diagn; 2006 May; 6(3):375-86. PubMed ID: 16706740
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 5. [Genetic characteristics of hearing disorders in changes in genes responsible for collagen synthesis].
    Markova TG
    Vestn Otorinolaringol; 2007; (3):17-21. PubMed ID: 17690651
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Genetic screening among children with congenital and early childhood hearing loss].
    Markova TG; Nekrasovan V MV; Shagina IA; Poliakov AA
    Vestn Otorinolaringol; 2006; (4):9-14. PubMed ID: 17152466
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Strategies and logistical requirements for efficient testing in genetic disease.
    Jackson-Cook C; Pandya A
    Clin Lab Med; 1995 Dec; 15(4):839-57. PubMed ID: 8838226
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Choice of rehabilitation in patients with mixed hypoacusis].
    Pogosov VS; Kapustina TA; Petrovskaia AN
    Vestn Otorinolaringol; 2001; (3):23-5. PubMed ID: 11510040
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Cavinton prevention of neurosensory hypoacousis in patients with different forms of tuberculosis].
    Maliavina US; Ovchinnikov IuM; Fasenko VP; Maliev BM; Kalinina MV; Dadasheva BB
    Vestn Otorinolaringol; 2003; (3):35-40. PubMed ID: 12847806
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Clinical genetics problems in pediatric practice].
    Mazurczak T
    Pediatr Pol; 1996 Mar; 71(3):183-90. PubMed ID: 8966088
    [TBL] [Abstract][Full Text] [Related]  

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

  • 12. DNA-based carrier screening in the Ashkenazi Jewish population.
    Zhang B; Dearing L; Amos J
    Expert Rev Mol Diagn; 2004 May; 4(3):377-92. PubMed ID: 15137904
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nonsyndromic hearing loss.
    Van Laer L; Cryns K; Smith RJ; Van Camp G
    Ear Hear; 2003 Aug; 24(4):275-88. PubMed ID: 12923419
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular basis of genetic disease and molecular methods.
    McPherson RA
    Clin Lab Med; 1995 Dec; 15(4):779-94. PubMed ID: 8838223
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Perspectives of molecular genetics of hearing disorders].
    Kempf HG; Brändle TU
    HNO; 1993 Feb; 41(2):68-76. PubMed ID: 8463117
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital and genetic sensorineural hearing loss.
    DiLeo MD; Amedee RG
    J La State Med Soc; 1993 Sep; 145(9):377-80. PubMed ID: 8263376
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Microwave therapy in combined rehabilitation of children suffering from chronic neurosensory hypoacusis].
    Uzunova AN; Kofanov RV; Chernysh NN
    Vopr Kurortol Fizioter Lech Fiz Kult; 2005; (4):28-30. PubMed ID: 16149415
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular diagnosis of neurosensory deafness: the gap between basic research and diagnostic application is increasing.
    Van Camp G
    Acta Otorhinolaryngol Belg; 2002; 56(4):337-40. PubMed ID: 12528250
    [No Abstract]   [Full Text] [Related]  

  • 19. [Experience in the use of current methods in early and differential diagnosis of hearing disorders].
    Ivanets IV; Muratov DL
    Vestn Otorinolaringol; 1995; (4):31-4. PubMed ID: 7676558
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Medico-genetic consultation for families with neurosensory hypoacusis of unknown etiology in both spouses].
    Bliumina MG
    Vestn Otorinolaringol; 1987; (4):33-5. PubMed ID: 3629805
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.