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Journal Abstract Search

148 related items for PubMed ID: 1952589

  • 1. Nonsyndromal profound genetic deafness in childhood.
    Cremers CW, Marres HA, van Rijn PM.
    Ann N Y Acad Sci; 1991; 630():191-6. PubMed ID: 1952589
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  • 3. Autosomal recessive nonsyndromic hearing loss.
    Sundstrom RA, Van Laer L, Van Camp G, Smith RJ.
    Am J Med Genet; 1999 Sep 24; 89(3):123-9. PubMed ID: 10704186
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  • 4. Autosomal dominant nonsyndromic hearing impairment.
    Van Laer L, McGuirt WT, Yang T, Smith RJ, Van Camp G.
    Am J Med Genet; 1999 Sep 24; 89(3):167-74. PubMed ID: 10704191
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  • 7. A genetic aetiological survey of severe childhood deafness in the United Arab Emirates.
    Al-Gazali LI.
    J Trop Pediatr; 1998 Jun 24; 44(3):157-60. PubMed ID: 9680781
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  • 12. [Hereditary deafness in Turkey. Initial results].
    Apaydin F, Pfister M, Iber M, Kandogan T, Leal SM, Brändle U, Cura O, Zenner HP.
    HNO; 1998 Sep 24; 46(9):809-14. PubMed ID: 9816535
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  • 15. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.
    Guilford P, Ben Arab S, Blanchard S, Levilliers J, Weissenbach J, Belkahia A, Petit C.
    Nat Genet; 1994 Jan 24; 6(1):24-8. PubMed ID: 8136828
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  • 16. Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan.
    Veske A, Oehlmann R, Younus F, Mohyuddin A, Müller-Myhsok B, Mehdi SQ, Gal A.
    Hum Mol Genet; 1996 Jan 24; 5(1):165-8. PubMed ID: 8789456
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  • 20. A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.
    Campbell DA, McHale DP, Brown KA, Moynihan LM, Houseman M, Karbani G, Parry G, Janjua AH, Newton V, al-Gazali L, Markham AF, Lench NJ, Mueller RF.
    J Med Genet; 1997 Dec 24; 34(12):1015-7. PubMed ID: 9429146
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