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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

177 related items for PubMed ID: 21514544

  • 21. A comparative study of hearing loss in two microdeletion syndromes: velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes.
    Zarchi O, Attias J, Raveh E, Basel-Vanagaite L, Saporta L, Gothelf D.
    J Pediatr; 2011 Feb; 158(2):301-6. PubMed ID: 20846670
    [Abstract] [Full Text] [Related]

  • 22. [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]

  • 23. 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
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  • 24. [Auditive function disturbances. Diagnostic orientation].
    Dauman R.
    Rev Prat; 2002 Oct 15; 52(16):1843-50. PubMed ID: 12564177
    [No Abstract] [Full Text] [Related]

  • 25. Sensorineural hearing loss in children.
    Wormald R, Viani L, Lynch SA, Green AJ.
    Ir Med J; 2010 Feb 15; 103(2):51-4. PubMed ID: 20666057
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  • 31. 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
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  • 37. [Hereditary hearing loss].
    Tropitzsch A, Schade-Mann T, Gamerdinger P.
    HNO; 2023 Feb 15; 71(2):131-142. PubMed ID: 36526931
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  • 39. Genetic hearing impairment.
    Ječmenica J, Bajec-Opančina A, Ječmenica D.
    Childs Nerv Syst; 2015 Apr 15; 31(4):515-9. PubMed ID: 25686889
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