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PUBMED FOR HANDHELDS

Journal Abstract Search

76 related items for PubMed ID: 9830215

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  • 3. X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery.
    Cremers CW, Hombergen GC, Scaf JJ, Huygen PL, Volkers WS, Pinckers AJ.
    Arch Otolaryngol; 1985 Apr; 111(4):249-54. PubMed ID: 3977755
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  • 4. Molecular analysis of the POU3F4 gene in patients with clinical and radiographic evidence of X-linked mixed deafness with perilymphatic gusher.
    Friedman RA, Bykhovskaya Y, Tu G, Talbot JM, Wilson DF, Parnes LS, Fischel-Ghodsian N.
    Ann Otol Rhinol Laryngol; 1997 Apr; 106(4):320-5. PubMed ID: 9109724
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  • 5. Computed tomographic diagnosis of X-linked congenital mixed deafness, fixation of the stapedial footplate, and perilymphatic gusher.
    Talbot JM, Wilson DF.
    Am J Otol; 1994 Mar; 15(2):177-82. PubMed ID: 8172298
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  • 6. Novel mutation in the homeobox domain of transcription factor POU3F4 associated with profound sensorineural hearing loss.
    Schild C, Prera E, Lüblinghoff N, Arndt S, Aschendorff A, Birkenhäger R.
    Otol Neurotol; 2011 Jun; 32(4):690-4. PubMed ID: 21555964
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  • 8. X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21.
    Piussan C, Hanauer A, Dahl N, Mathieu M, Kolski C, Biancalana V, Heyberger S, Strunski V.
    Am J Hum Genet; 1995 Jan; 56(1):224-30. PubMed ID: 7825582
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  • 9. The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK.
    Brunner HG, van Bennekom A, Lambermon EM, Oei TL, Cremers WR, Wieringa B, Ropers HH.
    Hum Genet; 1988 Dec; 80(4):337-40. PubMed ID: 2904400
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  • 14. Gusher in stapes surgery: a systematic review.
    Alicandri-Ciufelli M, Molinari G, Rosa MS, Monzani D, Presutti L.
    Eur Arch Otorhinolaryngol; 2019 Sep; 276(9):2363-2376. PubMed ID: 31273448
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  • 15. [Clinical and molecular genetic analysis of monozygotic twins displaying stapes gusher syndrome (DFN3)].
    Oh N, Kupka S, Mirghomizadeh F, Arold R, Zimmermann R, Blin N, Zenner HP, Pfister M.
    HNO; 2003 Aug; 51(8):629-33. PubMed ID: 12942177
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  • 16. Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafness.
    Reardon W, Roberts S, Phelps PD, Thomas NS, Beck L, Issac R, Hughes HE.
    Am J Med Genet; 1992 Nov 01; 44(4):513-7. PubMed ID: 1442898
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  • 17. Phenotype and genotype in females with POU3F4 mutations.
    Marlin S, Moizard MP, David A, Chaissang N, Raynaud M, Jonard L, Feldmann D, Loundon N, Denoyelle F, Toutain A.
    Clin Genet; 2009 Dec 01; 76(6):558-63. PubMed ID: 19930154
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  • 19. Clinical features of female heterozygotes in the X-linked mixed deafness syndrome (with perilymphatic gusher during stapes surgery).
    Cremers CW, Huygen PL.
    Int J Pediatr Otorhinolaryngol; 1983 Nov 01; 6(2):179-85. PubMed ID: 6662621
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  • 20. Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4.
    de Kok YJ, van der Maarel SM, Bitner-Glindzicz M, Huber I, Monaco AP, Malcolm S, Pembrey ME, Ropers HH, Cremers FP.
    Science; 1995 Feb 03; 267(5198):685-8. PubMed ID: 7839145
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