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

99 related items for PubMed ID: 3162715

  • 1. Linkage studies of Usher syndrome: analysis of an Acadian kindred in Louisiana.
    Pelias MZ, Lemoine DR, Kossar AL, Ward LJ, Wilson AF, Elston RC.
    Cytogenet Cell Genet; 1988; 47(1-2):111-2. PubMed ID: 3162715
    [No Abstract] [Full Text] [Related]

  • 2. Exclusion of Usher syndrome gene from much of chromosome 4.
    Smith RJ, Holcomb JD, Daiger SP, Caskey CT, Pelias MZ, Alford BR, Fontenot DD, Hejtmancik JF.
    Cytogenet Cell Genet; 1989; 50(2-3):102-6. PubMed ID: 2776474
    [Abstract] [Full Text] [Related]

  • 3. Genetic mapping of the gene for Usher syndrome: linkage analysis in a large Samaritan kindred.
    Bonné-Tamir B, Korostishevsky M, Kalinsky H, Seroussi E, Beker R, Weiss S, Godel V.
    Genomics; 1994 Mar 01; 20(1):36-42. PubMed ID: 8020954
    [Abstract] [Full Text] [Related]

  • 4. Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11.
    Keats BJ, Nouri N, Pelias MZ, Deininger PL, Litt M.
    Am J Hum Genet; 1994 Apr 01; 54(4):681-6. PubMed ID: 8128966
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Usher syndrome type I is not linked to D1S81 (pTHH 33): evidence for genetic heterogeneity.
    Kaplan J, Guasconi G, Bonneau D, Melki J, Briard ML, Munnich A, Dufier JL, Frézal J.
    Ann Genet; 1990 Oct 25; 33(2):105-8. PubMed ID: 1978628
    [Abstract] [Full Text] [Related]

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

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

  • 10. Linkage analysis in Usher syndrome type I (USH1) families from Spain.
    Espinós C, Nájera C, Millán JM, Ayuso C, Baiget M, Pérez-Garrigues H, Rodrigo O, Vilela C, Beneyto M.
    J Med Genet; 1998 May 25; 35(5):391-8. PubMed ID: 9610802
    [Abstract] [Full Text] [Related]

  • 11. 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 25; 35(8):666-7. PubMed ID: 9719374
    [Abstract] [Full Text] [Related]

  • 12. Genetic heterogeneity of Usher syndrome type II.
    Pieke Dahl S, Kimberling WJ, Gorin MB, Weston MD, Furman JM, Pikus A, Möller C.
    J Med Genet; 1993 Oct 25; 30(10):843-8. PubMed ID: 7901420
    [Abstract] [Full Text] [Related]

  • 13. Evidence against linkage of the gene for Usher's syndrome type 1 with group specific component (GC) on chromosome 4.
    Bonneau D, Kaplan J, Berthier M, Séger J, Dufier JL, Frézal J.
    Ann Genet; 1990 Oct 25; 33(2):103-4. PubMed ID: 2241083
    [Abstract] [Full Text] [Related]

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

  • 15. A genetic analysis of retinitis pigmentosa.
    Boughman JA, Fishman GA.
    Br J Ophthalmol; 1983 Jul 25; 67(7):449-54. PubMed ID: 6860611
    [Abstract] [Full Text] [Related]

  • 16. [From gene to disease; genetic causes of hearing loss and visual impairment sometimes accompanied by vestibular problems (Usher syndrome)].
    Pennings RJ, Kremer H, Deutman AF, Kimberling WJ, Cremers CW.
    Ned Tijdschr Geneeskd; 2002 Dec 07; 146(49):2354-8. PubMed ID: 12510399
    [Abstract] [Full Text] [Related]

  • 17. Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortium.
    Keats BJ, Todorov AA, Atwood LD, Pelias MZ, Hejtmancik JF, Kimberling WJ, Leppert M, Lewis RA, Smith RJ.
    Genomics; 1992 Nov 07; 14(3):707-14. PubMed ID: 1427898
    [Abstract] [Full Text] [Related]

  • 18. A mutation of PCDH15 among Ashkenazi Jews with the type 1 Usher syndrome.
    Ben-Yosef T, Ness SL, Madeo AC, Bar-Lev A, Wolfman JH, Ahmed ZM, Desnick RJ, Willner JP, Avraham KB, Ostrer H, Oddoux C, Griffith AJ, Friedman TB.
    N Engl J Med; 2003 Apr 24; 348(17):1664-70. PubMed ID: 12711741
    [No Abstract] [Full Text] [Related]

  • 19. Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene.
    Mansergh FC, Millington-Ward S, Kennan A, Kiang AS, Humphries M, Farrar GJ, Humphries P, Kenna PF.
    Am J Hum Genet; 1999 Apr 24; 64(4):971-85. PubMed ID: 10090882
    [Abstract] [Full Text] [Related]

  • 20. A DNA linkage study of Usher's syndrome excluding much of chromosome 4.
    Smith RJ.
    Laryngoscope; 1989 Sep 24; 99(9):940-9. PubMed ID: 2770384
    [Abstract] [Full Text] [Related]

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