These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

100 related items for PubMed ID: 10704186

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
    Riazuddin S, Nazli S, Ahmed ZM, Yang Y, Zulfiqar F, Shaikh RS, Zafar AU, Khan SN, Sabar F, Javid FT, Wilcox ER, Tsilou E, Boger ET, Sellers JR, Belyantseva IA, Riazuddin S, Friedman TB.
    Hum Mutat; 2008 Apr; 29(4):502-11. PubMed ID: 18181211
    [Abstract] [Full Text] [Related]

  • 23. Unconventional myosins and the genetics of hearing loss.
    Friedman TB, Sellers JR, Avraham KB.
    Am J Med Genet; 1999 Sep 24; 89(3):147-57. PubMed ID: 10704189
    [Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26. ARNSHL gene identification: past, present and future.
    Imtiaz A.
    Mol Genet Genomics; 2022 Sep 24; 297(5):1185-1193. PubMed ID: 35869994
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29. Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant.
    Bharadwaj T, Schrauwen I, Acharya A, Nouel-Saied LM, Väisänen ML, Kraatari M, Rahikkala E, Jarvela I, Kotimäki J, Leal SM.
    Mol Genet Genomic Med; 2022 Mar 24; 10(3):e1866. PubMed ID: 35150090
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Genetic causes of nonsyndromic hearing loss.
    Skvorak Giersch AB, Morton CC.
    Curr Opin Pediatr; 1999 Dec 24; 11(6):551-7. PubMed ID: 10590915
    [Abstract] [Full Text] [Related]

  • 33. Defective myosin VIIA gene responsible for Usher syndrome type 1B.
    Weil D, Blanchard S, Kaplan J, Guilford P, Gibson F, Walsh J, Mburu P, Varela A, Levilliers J, Weston MD.
    Nature; 1995 Mar 02; 374(6517):60-1. PubMed ID: 7870171
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4.
    Coyle B, Coffey R, Armour JA, Gausden E, Hochberg Z, Grossman A, Britton K, Pembrey M, Reardon W, Trembath R.
    Nat Genet; 1996 Apr 02; 12(4):421-3. PubMed ID: 8630497
    [Abstract] [Full Text] [Related]

  • 38. Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q.
    Fukushima K, Ramesh A, Srisailapathy CR, Ni L, Chen A, O'Neill M, Van Camp G, Coucke P, Smith SD, Kenyon JB.
    Hum Mol Genet; 1995 Sep 02; 4(9):1643-8. PubMed ID: 8541854
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 5.