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Journal Abstract Search

120 related items for PubMed ID: 1623624

  • 1. A syndrome of progressive sensorineural deafness and cataract inherited as an autosomal dominant trait.
    Guala A, Germinetti V, Sebastiani F, Silengo MC.
    Clin Genet; 1992 Jun; 41(6):293-5. PubMed ID: 1623624
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  • 2. Cochleosaccular degeneration of the inner ear and progressive cataracts inherited as an autosomal dominant trait.
    Nadol JB, Burgess B.
    Laryngoscope; 1982 Sep; 92(9 Pt 1):1028-37. PubMed ID: 7121157
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  • 3. [Genetic study of sensorineural hearing loss].
    Bliumina MG, Moskovkina AG.
    Genetika; 1982 Sep; 18(6):1012-7. PubMed ID: 7201942
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  • 5. Autosomal dominant palmoplantar hyperkeratosis and sensorineural deafness in three generations.
    Sharland M, Bleach NR, Goberdhan PD, Patton MA.
    J Med Genet; 1992 Jan; 29(1):50-2. PubMed ID: 1532426
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  • 6. Progressive autosomal dominant optic atrophy and sensorineural hearing loss in a Turkish family.
    Ozden S, Düzcan F, Wollnik B, Cetin OG, Sahiner T, Bayramoğlu I, Yüksel-Apak M, Bağci H.
    Ophthalmic Genet; 2002 Mar; 23(1):29-36. PubMed ID: 11910556
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  • 8. Three members of a family with pili torti and sensorineural hearing loss: the Bjornstad syndrome.
    Richards KA, Mancini AJ.
    J Am Acad Dermatol; 2002 Feb; 46(2):301-3. PubMed ID: 11807445
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  • 9. Heterogeneity of dominant high-frequency sensorineural deafness.
    Higashi K.
    Clin Genet; 1988 Jun; 33(6):424-8. PubMed ID: 3168315
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  • 15. 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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