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Journal Abstract Search

171 related items for PubMed ID: 24475916

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  • 6. Partial duplication of chromosome 19 associated with syndromic duane retraction syndrome.
    Abu-Amero KK, Kondkar AA, Al Otaibi A, Alorainy IA, Khan AO, Hellani AM, Oystreck DT, Bosley TM.
    Ophthalmic Genet; 2015 Mar; 36(1):14-20. PubMed ID: 23952617
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  • 7. Magnetic resonance imaging evidence for widespread orbital dysinnervation in dominant Duane's retraction syndrome linked to the DURS2 locus.
    Demer JL, Clark RA, Lim KH, Engle EC.
    Invest Ophthalmol Vis Sci; 2007 Jan; 48(1):194-202. PubMed ID: 17197533
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  • 8. A novel form of aberrant innervation in congenital cranial dysinnervation disorder.
    Khan AO.
    J AAPOS; 2009 Feb; 13(1):105-6. PubMed ID: 18930669
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  • 11. Imaging findings in congenital cranial dysinnervation disorders.
    Ferreira RM, Amaral LL, Gonçalves MV, Lin K.
    Top Magn Reson Imaging; 2011 Dec; 22(6):283-94. PubMed ID: 24132067
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  • 14. Partial chromosome 7 duplication with a phenotype mimicking the HOXA1 spectrum disorder.
    Abu-Amero KK, Kondkar AA, Salih MA, Alorainy IA, Khan AO, Oystreck DT, Bosley TM.
    Ophthalmic Genet; 2013 Dec; 34(1-2):90-6. PubMed ID: 22950449
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  • 18. Ocular manifestations of 22q11.2 microduplication.
    Cordovez JA, Capasso J, Lingao MD, Sadagopan KA, Spaeth GL, Wasserman BN, Levin AV.
    Ophthalmology; 2014 Jan; 121(1):392-398. PubMed ID: 23972321
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