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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

168 related items for PubMed ID: 10208263

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  • 3. Sector Retinitis Pigmentosa Associated With Novel Compound Heterozygous Mutations of CDH23.
    Branson SV, McClintic JI, Stamper TH, Haldeman-Englert CR, John VJ.
    Ophthalmic Surg Lasers Imaging Retina; 2016 Feb; 47(2):183-6. PubMed ID: 26878454
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  • 5. Hearing loss in Usher syndrome type II is nonprogressive.
    Reisser CF, Kimberling WJ, Otterstedde CR.
    Ann Otol Rhinol Laryngol; 2002 Dec; 111(12 Pt 1):1108-11. PubMed ID: 12498372
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  • 11. The combination of vestibular impairment and congenital sensorineural hearing loss predisposes patients to ocular anomalies, including Usher syndrome.
    Kletke S, Batmanabane V, Dai T, Vincent A, Li S, Gordon KA, Papsin BC, Cushing SL, Héon E.
    Clin Genet; 2017 Jul; 92(1):26-33. PubMed ID: 27743452
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  • 12. Is there genetic heterogeneity in Usher's syndrome?
    Matthews TW, Poliquin J, Mount J, MacFie D.
    J Otolaryngol; 1987 Mar; 16(2):61-6. PubMed ID: 3599157
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  • 19. Variable clinical features in patients with CDH23 mutations (USH1D-DFNB12).
    Pennings RJ, Topsakal V, Astuto L, de Brouwer AP, Wagenaar M, Huygen PL, Kimberling WJ, Deutman AF, Kremer H, Cremers CW.
    Otol Neurotol; 2004 Sep; 25(5):699-706. PubMed ID: 15353998
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