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

88 related items for PubMed ID: 9639681

  • 1. Assembly of a high-resolution map of the Acadian Usher syndrome region and localization of the nuclear EF-hand acidic gene.
    DeAngelis MM, Doucet JP, Drury S, Sherry ST, Robichaux MB, Den Z, Pelias MZ, Ditta GM, Keats BJ, Deininger PL, Batzer MA.
    Biochim Biophys Acta; 1998 Jul 01; 1407(1):84-91. PubMed ID: 9639681
    [Abstract] [Full Text] [Related]

  • 2. Fine mapping of the usher syndrome type IC to chromosome 11p14 and identification of flanking markers by haplotype analysis.
    Ayyagari R, Li Y, Smith RJ, Pelias MZ, Hejtmancik JF.
    Mol Vis; 1995 Oct 25; 1():2. PubMed ID: 9238080
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. USH1C: a rare cause of USH1 in a non-Acadian population and a founder effect of the Acadian allele.
    Ouyang XM, Hejtmancik JF, Jacobson SG, Xia XJ, Li A, Du LL, Newton V, Kaiser M, Balkany T, Nance WE, Liu XZ.
    Clin Genet; 2003 Feb 25; 63(2):150-3. PubMed ID: 12630964
    [Abstract] [Full Text] [Related]

  • 5. Two families from New England with usher syndrome type IC with distinct haplotypes.
    DeAngelis MM, McGee TL, Keats BJ, Slim R, Berson EL, Dryja TP.
    Am J Ophthalmol; 2001 Mar 25; 131(3):355-8. PubMed ID: 11239869
    [Abstract] [Full Text] [Related]

  • 6. Refined mapping of the Usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous region.
    Joensuu T, Blanco G, Pakarinen L, Sistonen P, Kääriäinen H, Brown S, Chapelle A, Sankila EM.
    Genomics; 1996 Dec 15; 38(3):255-63. PubMed ID: 8975700
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. The USH1C 216G-->A mutation and the 9-repeat VNTR(t,t) allele are in complete linkage disequilibrium in the Acadian population.
    Savas S, Frischhertz B, Pelias MZ, Batzer MA, Deininger PL, Keats BB.
    Hum Genet; 2002 Jan 15; 110(1):95-7. PubMed ID: 11810303
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10.
    Wayne S, Der Kaloustian VM, Schloss M, Polomeno R, Scott DA, Hejtmancik JF, Sheffield VC, Smith RJ.
    Hum Mol Genet; 1996 Oct 15; 5(10):1689-92. PubMed ID: 8894709
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Usher syndrome: definition and estimate of prevalence from two high-risk populations.
    Boughman JA, Vernon M, Shaver KA.
    J Chronic Dis; 1983 Oct 15; 36(8):595-603. PubMed ID: 6885960
    [Abstract] [Full Text] [Related]

  • 16. A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2.
    Hmani M, Ghorbel A, Boulila-Elgaied A, Ben Zina Z, Kammoun W, Drira M, Chaabouni M, Petit C, Ayadi H.
    Eur J Hum Genet; 1999 Apr 15; 7(3):363-7. PubMed ID: 10234513
    [Abstract] [Full Text] [Related]

  • 17. [Genetic research on Usher's syndrome in Spain].
    Espinós C, Millán JM.
    Med Clin (Barc); 1998 Mar 14; 110(9):340-1. PubMed ID: 9567267
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Construction of a YAC contig encompassing the Usher syndrome type 1C and familial hyperinsulinism loci on chromosome 11p14-15.1.
    Ayyagari R, Nestorowicz A, Li Y, Chandrasekharappa S, Chinault C, van Tuinen P, Smith RJ, Hejtmancik JF, Permutt MA.
    Genome Res; 1996 Jun 14; 6(6):504-14. PubMed ID: 8828039
    [Abstract] [Full Text] [Related]

  • 20. Usher syndrome type III (USH3) linked to chromosome 3q in an Italian family.
    Gasparini P, De Fazio A, Croce AI, Stanziale P, Zelante L.
    J Med Genet; 1998 Aug 14; 35(8):666-7. PubMed ID: 9719374
    [Abstract] [Full Text] [Related]

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