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PUBMED FOR HANDHELDS

Journal Abstract Search

84 related items for PubMed ID: 646734

  • 1. Dominantly inherited low-frequency hearing loss.
    Parving A, Johnsen NJ, Holm-Jensen S.
    Audiology; 1978; 17(2):165-72. PubMed ID: 646734
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  • 5. Clinical findings and diagnostic problems in sensorineural low frequency hearing loss.
    Parving A, Bak-Pedersen K.
    Acta Otolaryngol; 1978; 85(3-4):184-90. PubMed ID: 636868
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  • 8. Gingival fibromatosis with sensorineural hearing loss: an autosomal dominant trait.
    Hartsfield JK, Bixler D, Hazen RH.
    Am J Med Genet; 1985 Nov; 22(3):623-7. PubMed ID: 4061496
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  • 12. The autosomal dominant syndrome of progressive optic atrophy and congenital deafness.
    Kollarits CR, Pinheiro ML, Swann ER, Marcus DF, Corrie WS.
    Am J Ophthalmol; 1979 Jun; 87(6):789-92. PubMed ID: 453309
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  • 13. Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF.
    Smith SD, Kelley PM, Kenyon JB, Hoover D.
    J Med Genet; 2000 Jun; 37(6):446-8. PubMed ID: 10851256
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  • 18. The DFNA10 phenotype.
    De Leenheer EM, Huygen PL, Wayne S, Smith RJ, Cremers CW.
    Ann Otol Rhinol Laryngol; 2001 Sep; 110(9):861-6. PubMed ID: 11558763
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