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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

644 related items for PubMed ID: 10729113

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  • 3. Spectrum of mutations in USH2A in British patients with Usher syndrome type II.
    Leroy BP, Aragon-Martin JA, Weston MD, Bessant DA, Willis C, Webster AR, Bird AC, Kimberling WJ, Payne AM, Bhattacharya SS.
    Exp Eye Res; 2001 May; 72(5):503-9. PubMed ID: 11311042
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  • 6. Prevalence of 2314delG mutation in Spanish patients with Usher syndrome type II (USH2).
    Beneyto MM, Cuevas JM, Millán JM, Espinós C, Mateu E, González-Cabo P, Baiget M, Doménech M, Bernal S, Ayuso C, García-Sandoval B, Trujillo MJ, Borrego S, Antiñolo G, Carballo M, Nájera C.
    Ophthalmic Genet; 2000 Jun; 21(2):123-8. PubMed ID: 10916187
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  • 8. Seven novel mutations in the long isoform of the USH2A gene in Chinese families with nonsyndromic retinitis pigmentosa and Usher syndrome Type II.
    Xu W, Dai H, Lu T, Zhang X, Dong B, Li Y.
    Mol Vis; 2011 Jun; 17():1537-52. PubMed ID: 21686329
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  • 10. [Mutational frequencies in usherin(USH2A gene) in 26 Colombian individuals with Usher syndrome type II].
    López G, Gelvez NY, Tamayo M.
    Biomedica; 2011 Mar; 31(1):82-90. PubMed ID: 22159486
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  • 11. Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II.
    Yan D, Ouyang X, Patterson DM, Du LL, Jacobson SG, Liu XZ.
    J Hum Genet; 2009 Dec; 54(12):732-8. PubMed ID: 19881469
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  • 15. Identification of five novel mutations in the long isoform of the USH2A gene in Chinese families with Usher syndrome type II.
    Dai H, Zhang X, Zhao X, Deng T, Dong B, Wang J, Li Y.
    Mol Vis; 2008 Dec; 14():2067-75. PubMed ID: 19023448
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  • 16. Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing loss.
    Rivolta C, Sweklo EA, Berson EL, Dryja TP.
    Am J Hum Genet; 2000 Jun; 66(6):1975-8. PubMed ID: 10775529
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