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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

102 related items for PubMed ID: 21510145

  • 1. Phenotypes of two Dutch DFNA3 families with mutations in GJB2.
    Weegerink NJ, Pennings RJ, Huygen PL, Hoefsloot LH, Cremers CW, Kunst HP.
    Ann Otol Rhinol Laryngol; 2011 Mar; 120(3):191-7. PubMed ID: 21510145
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  • 4. Phenotype/genotype correlations in a DFNB1 cohort with ethnical diversity.
    Angeli SI.
    Laryngoscope; 2008 Nov; 118(11):2014-23. PubMed ID: 18758381
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  • 10. Hearing loss associated with an unusual mutation combination in the gap junction beta 2 (GJB2) gene in a Chinese family.
    Huang A, Yuan Y, Duan N, Jiang X, Wang B, Liu Y, Kang D, Zhang X, Zhu Q, Dai P.
    Int J Pediatr Otorhinolaryngol; 2014 Apr; 78(4):599-603. PubMed ID: 24503448
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  • 12. Longitudinal phenotypic analysis in patients with connexin 26 (GJB2) (DFNB1) and connexin 30 (GJB6) mutations.
    Stinckens C, Kremer H, van Wijk E, Hoefsloot LH, Huygen PL, Standaert L, Fryns JP, Cremers CW.
    Ann Otol Rhinol Laryngol; 2004 Jul; 113(7):587-93. PubMed ID: 15274422
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  • 14. GJB2 mutations: Genotypic and phenotypic correlation in a cohort of 690 hearing-impaired patients, toward a new mutation?
    Leclère JC, Le Gac MS, Le Maréchal C, Ferec C, Marianowski R.
    Int J Pediatr Otorhinolaryngol; 2017 Nov; 102():80-85. PubMed ID: 29106882
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  • 19. Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcome.
    Riahi Z, Zainine R, Mellouli Y, Hannachi R, Bouyacoub Y, Laroussi N, Beltaief N, Kefi R, Romdhane L, Bonnet C, Abdelhak S, Besbes G.
    Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1481-4. PubMed ID: 23856378
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  • 20. Genotypic and phenotypic correlations of DFNB1-related hearing impairment in the Midwestern United States.
    Lim LH, Bradshaw JK, Guo Y, Pilipenko V, Madden C, Ingala D, Keddache M, Choo DI, Wenstrup R, Greinwald JH.
    Arch Otolaryngol Head Neck Surg; 2003 Aug; 129(8):836-40. PubMed ID: 12925341
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