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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 1952611)

  • 1. Ascertainment of families with hereditary deafness for linkage studies. Waardenburg and Usher syndromes.
    Stevens C; Arnos K; Bodurtha J; Wright L; Rawlings B; Marazita M; Nance W; Diehl S
    Ann N Y Acad Sci; 1991; 630():293-4. PubMed ID: 1952611
    [No Abstract]   [Full Text] [Related]  

  • 2. Hereditary congenital severe deafness syndromes.
    Konigsmark BW
    Ann Otol Rhinol Laryngol; 1971 Apr; 80(2):269-88. PubMed ID: 4927796
    [No Abstract]   [Full Text] [Related]  

  • 3. 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; 14(3):707-14. PubMed ID: 1427898
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic diseases of hearing.
    Spillmann T
    Curr Opin Neurol; 1994 Feb; 7(1):81-7. PubMed ID: 8173684
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Estimation of prognosis and prevalence of retinitis pigmentosa and Usher syndrome in Norway.
    Grøndahl J
    Clin Genet; 1987 Apr; 31(4):255-64. PubMed ID: 3594933
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mapping and cloning hereditary deafness genes.
    Cremers FP; Bitner-Glindzicz M; Pembrey ME; Ropers HH
    Curr Opin Genet Dev; 1995 Jun; 5(3):371-5. PubMed ID: 7549433
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Report on attempts to localize Usher syndrome type 1 by linkage analysis to selected candidate regions.
    Pieke Dahl S; Weston MD; Kimberling WJ; Kenyon JB; Shugart YY; Smith RJ
    Ann N Y Acad Sci; 1991; 630():298-300. PubMed ID: 1952612
    [No Abstract]   [Full Text] [Related]  

  • 8. Localization of a gene for Waardenburg syndrome type I.
    Read AP; Foy C; Newton V; Harris R
    Ann N Y Acad Sci; 1991; 630():143-51. PubMed ID: 1952585
    [No Abstract]   [Full Text] [Related]  

  • 9. Confirmation of the location of a Waardenburg syndrome type I mutation on human chromosome 2q. Tight linkage to FN1 and ALPP.
    Asher JH; Morell R; Friedman TB
    Ann N Y Acad Sci; 1991; 630():295-7. PubMed ID: 1683205
    [No Abstract]   [Full Text] [Related]  

  • 10. A progress report on the localization of Usher syndrome type II to chromosome 1q.
    Weston MD; Kimberling WJ; Möller CG; Pieke Dahl S; Smith RJ; Martini A; Milani M
    Ann N Y Acad Sci; 1991; 630():284-7. PubMed ID: 1952607
    [No Abstract]   [Full Text] [Related]  

  • 11. Distinctive audiometric features between USH2A and USH2B subtypes of Usher syndrome.
    Hmani-Aifa M; Ben Arab S; Kharrat K; Orten DJ; Boulila-Elgaied A; Drira M; Hachicha S; Kimberling WJ; Ayadi H
    J Med Genet; 2002 Apr; 39(4):281-3. PubMed ID: 11950859
    [No Abstract]   [Full Text] [Related]  

  • 12. Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF.
    Smith SD; Kelley PM; Kenyon JB; Hoover D
    J Med Genet; 2000 Jun; 37(6):446-8. PubMed ID: 10851256
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Histopathologic findings of the inner ears with Alport, Usher and Waardenburg syndromes.
    Takasaki K; Balaban CD; Sando I
    Adv Otorhinolaryngol; 2000; 56():218-32. PubMed ID: 10868239
    [No Abstract]   [Full Text] [Related]  

  • 14. The hereditary syndrome of congenital deafness and retinitis pigmentosa. (Usher's syndrome).
    Kloepfer HW; Laguaite JK
    Laryngoscope; 1966 May; 76(5):850-62. PubMed ID: 5937908
    [No Abstract]   [Full Text] [Related]  

  • 15. Genetic studies of Usher syndrome.
    Kimberling WJ; Weston MD; Pieke Dahl S; Kenyon JB; Shugart YY; Moller C; Davenport SL; Martini A; Milani M; Smith RJ
    Ann N Y Acad Sci; 1991; 630():167-75. PubMed ID: 1952588
    [No Abstract]   [Full Text] [Related]  

  • 16. [Paranoid psychosis in congenital deafness and retinopathia pigmentosa (Usher syndrome), case report].
    Eikmeier G; Dieffenbach R
    Nervenarzt; 1984 May; 55(5):269-70. PubMed ID: 6462296
    [No Abstract]   [Full Text] [Related]  

  • 17. Childhood deafness in Cape Town.
    Sellars S; Napier E; Beighton P
    S Afr Med J; 1975 Jul; 49(28):1135-8. PubMed ID: 1154167
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic heterogeneity of Usher syndrome.
    Kimberling WJ; Orten D; Pieke-Dahl S
    Adv Otorhinolaryngol; 2000; 56():11-8. PubMed ID: 10868209
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Usher syndrome and possible heredity linked to X chromosome].
    Baldellou Vázquez A; Navarro Zapata C; Albalad Cebrian E; Mateo Blanco A
    An Esp Pediatr; 1993 Nov; 39(5):462-4. PubMed ID: 8285470
    [No Abstract]   [Full Text] [Related]  

  • 20. Genetic heterogeneity of Usher syndrome type II in a Dutch population.
    Pieke-Dahl S; van Aarem A; Dobin A; Cremers CW; Kimberling WJ
    J Med Genet; 1996 Sep; 33(9):753-7. PubMed ID: 8880575
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.