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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

186 related items for PubMed ID: 27440999

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  • 3. Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%.
    Roux AF, Faugère V, Le Guédard S, Pallares-Ruiz N, Vielle A, Chambert S, Marlin S, Hamel C, Gilbert B, Malcolm S, Claustres M, French Usher Syndrome Collaboration.
    J Med Genet; 2006 Sep; 43(9):763-8. PubMed ID: 16679490
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  • 9. Cochlear implantation in individuals with Usher type 1 syndrome.
    Liu XZ, Angeli SI, Rajput K, Yan D, Hodges AV, Eshraghi A, Telischi FF, Balkany TJ.
    Int J Pediatr Otorhinolaryngol; 2008 Jun; 72(6):841-7. PubMed ID: 18395802
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  • 10. Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes.
    Schultz JM, Bhatti R, Madeo AC, Turriff A, Muskett JA, Zalewski CK, King KA, Ahmed ZM, Riazuddin S, Ahmad N, Hussain Z, Qasim M, Kahn SN, Meltzer MR, Liu XZ, Munisamy M, Ghosh M, Rehm HL, Tsilou ET, Griffith AJ, Zein WM, Brewer CC, Riazuddin S, Friedman TB.
    J Med Genet; 2011 Nov; 48(11):767-75. PubMed ID: 21940737
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  • 13. The Genetics of Usher Syndrome in the Israeli and Palestinian Populations.
    Khalaileh A, Abu-Diab A, Ben-Yosef T, Raas-Rothschild A, Lerer I, Alswaiti Y, Chowers I, Banin E, Sharon D, Khateb S.
    Invest Ophthalmol Vis Sci; 2018 Feb 01; 59(2):1095-1104. PubMed ID: 29490346
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  • 19. Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients.
    Riahi Z, Bonnet C, Zainine R, Lahbib S, Bouyacoub Y, Bechraoui R, Marrakchi J, Hardelin JP, Louha M, Largueche L, Ben Yahia S, Kheirallah M, Elmatri L, Besbes G, Abdelhak S, Petit C.
    PLoS One; 2015 Feb 01; 10(3):e0120584. PubMed ID: 25798947
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