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PUBMED FOR HANDHELDS

Journal Abstract Search


334 related items for PubMed ID: 19203801

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  • 23. Audiologic and otologic characteristics of Pfeiffer syndrome.
    Vallino-Napoli LD.
    Cleft Palate Craniofac J; 1996 Nov; 33(6):524-9. PubMed ID: 8939381
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  • 24. Audiologic findings in Pfeiffer syndrome.
    Desai U, Rosen H, Mulliken JB, Gopen Q, Meara JG, Rogers GF.
    J Craniofac Surg; 2010 Sep; 21(5):1411-8. PubMed ID: 20856029
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  • 29. Craniofacial features in Goldenhar syndrome.
    Vinay C, Reddy RS, Uloopi KS, Madhuri V, Sekhar RC.
    J Indian Soc Pedod Prev Dent; 2009 Sep; 27(2):121-4. PubMed ID: 19736507
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  • 30. The effects of Goldenhar Syndrome on hearing and speech development.
    Zizlavsky S, Anam K, Suwento R, Rahmawati I.
    Med J Malaysia; 2021 Nov; 76(6):946-949. PubMed ID: 34806693
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  • 31. Hearing impairment and ear anomalies in craniofacial microsomia: a systematic review.
    Rooijers W, Tio PAE, van der Schroeff MP, Padwa BL, Dunaway DJ, Forrest CR, Koudstaal MJ, Caron CJJM.
    Int J Oral Maxillofac Surg; 2022 Oct; 51(10):1296-1304. PubMed ID: 35125269
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  • 35. Isolated microtia as a marker for unsuspected hemifacial microsomia.
    Keogh IJ, Troulis MJ, Monroy AA, Eavey RD, Kaban LB.
    Arch Otolaryngol Head Neck Surg; 2007 Oct; 133(10):997-1001. PubMed ID: 17938322
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  • 36. [Malformation processes in the middle ear. Branchio-oto-renal syndrome (BOR)].
    Motta G, Mesolella M, Salafia M.
    Acta Otorhinolaryngol Ital; 1996 Apr; 16(2 Suppl 53):42-6. PubMed ID: 8928671
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  • 37. Hearing characterization in oculoauriculovertebral spectrum: A prospective study with 10 patients.
    Goetze TB, Sleifer P, Rosa RF, da Silva AP, Graziadio C, Zen PR.
    Am J Med Genet A; 2017 Feb; 173(2):309-314. PubMed ID: 27774762
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  • 40. Congenital facial neuropathy in oculoauriculovertebral dysplasia-hemifacial microsomia (Goldenhar-Gorlin syndrome).
    Aleksic S, Budzilovich G, Reuben R, Sekhar HC, Feigin I, Finegold M, Boal D, Tokita N, Converse JM.
    Bull Los Angeles Neurol Soc; 1976 Apr; 41(2):68-77. PubMed ID: 1030652
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