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PUBMED FOR HANDHELDS

Journal Abstract Search


174 related items for PubMed ID: 21397065

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  • 4. Biometric and molecular characterization of clinically diagnosed posterior microphthalmos.
    Nowilaty SR, Khan AO, Aldahmesh MA, Tabbara KF, Al-Amri A, Alkuraya FS.
    Am J Ophthalmol; 2013 Feb; 155(2):361-372.e7. PubMed ID: 23127749
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  • 7. Novel mutations in MFRP and PRSS56 are associated with posterior microphthalmos.
    Bacci GM, Bargiacchi S, Fortunato P, Pisaneschi E, Peluso F, Marziali E, Magli A, Giglio SR, Caputo R.
    Ophthalmic Genet; 2020 Feb; 41(1):49-56. PubMed ID: 32118495
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  • 8. Gene profiling of postnatal Mfrprd6 mutant eyes reveals differential accumulation of Prss56, visual cycle and phototransduction mRNAs.
    Soundararajan R, Won J, Stearns TM, Charette JR, Hicks WL, Collin GB, Naggert JK, Krebs MP, Nishina PM.
    PLoS One; 2014 Feb; 9(10):e110299. PubMed ID: 25357075
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  • 9. Identification of MFRP and the secreted serine proteases PRSS56 and ADAMTS19 as part of a molecular network involved in ocular growth regulation.
    Koli S, Labelle-Dumais C, Zhao Y, Paylakhi S, Nair KS.
    PLoS Genet; 2021 Mar; 17(3):e1009458. PubMed ID: 33755662
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  • 16. Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness.
    Masmoudi S, Antonarakis SE, Schwede T, Ghorbel AM, Gratri M, Pappasavas MP, Drira M, Elgaied-Boulila A, Wattenhofer M, Rossier C, Scott HS, Ayadi H, Guipponi M.
    Hum Mutat; 2001 Aug; 18(2):101-8. PubMed ID: 11462234
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  • 18. Evaluation of PRSS56 in Chinese subjects with high hyperopia or primary angle-closure glaucoma.
    Jiang D, Yang Z, Li S, Xiao X, Jia X, Wang P, Guo X, Liu X, Zhang Q.
    Mol Vis; 2013 Aug; 19():2217-26. PubMed ID: 24227917
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