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 *

245 related articles for article (PubMed ID: 6885960)

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

  • 2. Usher syndrome: results of a screening program in Colombia.
    Tamayo ML; Bernal JE; Tamayo GE; Frias JL; Alvira G; Vergara O; Rodriguez V; Uribe JI; Silva JC
    Clin Genet; 1991 Oct; 40(4):304-11. PubMed ID: 1756603
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

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

  • 5. Prevalence and geographical distribution of Usher syndrome in Germany.
    Spandau UH; Rohrschneider K
    Graefes Arch Clin Exp Ophthalmol; 2002 Jun; 240(6):495-8. PubMed ID: 12107518
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and genetic linkage analysis of a large Venezuelan kindred with Usher syndrome.
    Keogh IJ; Godinho RN; Wu TP; Diaz de Palacios AM; Palacios N; Bello de Alford M; De Almada MI; MarPalacios N; Vazquez A; Mattei R; Seidman C; Seidman J; Eavey RD
    Int J Pediatr Otorhinolaryngol; 2004 Aug; 68(8):1063-8. PubMed ID: 15236894
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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; 146(49):2354-8. PubMed ID: 12510399
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comprehensive molecular diagnosis of a large cohort of Japanese retinitis pigmentosa and Usher syndrome patients by next-generation sequencing.
    Oishi M; Oishi A; Gotoh N; Ogino K; Higasa K; Iida K; Makiyama Y; Morooka S; Matsuda F; Yoshimura N
    Invest Ophthalmol Vis Sci; 2014 Oct; 55(11):7369-75. PubMed ID: 25324289
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 1407(1):84-91. PubMed ID: 9639681
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Usher syndrome in the Lebanese population and further refinement of the USH2A candidate region.
    Saouda M; Mansour A; Bou Moglabey Y; El Zir E; Mustapha M; Chaib H; Nehmé A; Mégarbané A; Loiselet J; Petit C; Slim R
    Hum Genet; 1998 Aug; 103(2):193-8. PubMed ID: 9760205
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The prevalence of Usher syndrome and other retinal dystrophy-hearing impairment associations.
    Rosenberg T; Haim M; Hauch AM; Parving A
    Clin Genet; 1997 May; 51(5):314-21. PubMed ID: 9212179
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [The incidence of Usher's syndrome and its clinical types].
    Bereketoğlu M; Avşar EU; Turan O; Afrashi F; Apaydin F
    Kulak Burun Bogaz Ihtis Derg; 2002; 9(1):15-20. PubMed ID: 12122620
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability.
    Aller E; Jaijo T; Oltra S; Alió J; Galán F; Nájera C; Beneyto M; Millán JM
    Clin Genet; 2004 Dec; 66(6):525-9. PubMed ID: 15521980
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early diagnosis of Usher syndrome in children.
    Mets MB; Young NM; Pass A; Lasky JB
    Trans Am Ophthalmol Soc; 2000; 98():237-42; discussion 243-5. PubMed ID: 11190026
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 33(2):105-8. PubMed ID: 1978628
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Usher syndrome in the city of Birmingham--prevalence and clinical classification.
    Hope CI; Bundey S; Proops D; Fielder AR
    Br J Ophthalmol; 1997 Jan; 81(1):46-53. PubMed ID: 9135408
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss.
    Ebermann I; Scholl HP; Charbel Issa P; Becirovic E; Lamprecht J; Jurklies B; Millán JM; Aller E; Mitter D; Bolz H
    Hum Genet; 2007 Apr; 121(2):203-11. PubMed ID: 17171570
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Perform vestibular test among all small deaf children! Early detection of Usher syndrome improves the possibilities of communication in the event of later deaf-blindness].
    Konrádsson K; Magnusson M; Andréasson S
    Lakartidningen; 1998 Jan; 95(5):379-81. PubMed ID: 9492482
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Bronchial asthma in a patient with Usher syndrome: case report.
    Baris B; Ataman M; Sener C; Kalyoncu F
    J Asthma; 1994; 31(6):487-90. PubMed ID: 7961327
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.