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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

134 related items for PubMed ID: 17567887

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  • 3. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 Brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling.
    Batissoco AC, Abreu-Silva RS, Braga MC, Lezirovitz K, Della-Rosa V, Alfredo T, Otto PA, Mingroni-Netto RC.
    Ear Hear; 2009 Feb; 30(1):1-7. PubMed ID: 19125024
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  • 4. [Prevalence of the 35delG mutation in the GJB2 gene, del (GJB6-D13S1830) in the GJB6 gene, Q829X in the OTOF gene and A1555G in the mitochondrial 12S rRNA gene in subjects with non-syndromic sensorineural hearing impairment of congenital/childhood onset].
    Gallo-Terán J, Morales-Angulo C, Rodríguez-Ballesteros M, Moreno-Pelayo MA, del Castillo I, Moreno F.
    Acta Otorrinolaringol Esp; 2005 Dec; 56(10):463-8. PubMed ID: 16425640
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  • 5. Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern Austria.
    Frei K, Ramsebner R, Lucas T, Baumgartner WD, Schoefer C, Wachtler FJ, Kirschhofer K.
    Hear Res; 2004 Oct; 196(1-2):115-8. PubMed ID: 15464308
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  • 11. [Pseudodominants of two recessive connexin mutations in non-syndromic sensorineural hearing loss?].
    Birkenhäger R, Zimmer AJ, Maier W, Schipper J.
    Laryngorhinootologie; 2006 Mar; 85(3):191-6. PubMed ID: 16547895
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  • 12. Etiology of unilateral hearing loss in a national hereditary deafness repository.
    Dodson KM, Georgolios A, Barr N, Nguyen B, Sismanis A, Arnos KS, Norris VW, Chapman D, Nance WE, Pandya A.
    Am J Otolaryngol; 2012 Mar; 33(5):590-4. PubMed ID: 22534022
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  • 13. Genetic Aetiology of Nonsyndromic Hearing Loss in Moravia-Silesia.
    Plevova P, Tvrda P, Paprskarova M, Turska P, Kantorova B, Mrazkova E, Zapletalova J.
    Medicina (Kaunas); 2018 May 04; 54(2):. PubMed ID: 30344259
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  • 15. Unique spectrum of GJB2 mutations in Mexico.
    de la Luz Arenas-Sordo M, Menendez I, Hernández-Zamora E, Sirmaci A, Gutiérrez-Tinajero D, McGetrick M, Murphy-Ruiz P, Leyva-Juárez X, Huesca-Hernández F, Dominguez-Aburto J, Tekin M.
    Int J Pediatr Otorhinolaryngol; 2012 Nov 04; 76(11):1678-80. PubMed ID: 22925408
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  • 16. Molecular study in Brazilian cochlear implant recipients.
    Christiani TV, Alexandrino F, de Oliveira CA, Amantini RC, Bevilacqua MC, Filho OA, Porto P, Sartorato EL.
    Am J Med Genet A; 2007 Jul 15; 143A(14):1580-2. PubMed ID: 17567889
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  • 19. [Etiologic analysis of severe to profound hearing loss patients from Chifeng city in Inner Mongolia].
    Yuan YY, Dai P, Zhu XH, Kang DY, Zhang X, Huang DL.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2009 Apr 15; 44(4):292-6. PubMed ID: 19558834
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