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Journal Abstract Search

248 related items for PubMed ID: 17333094

  • 21. Molecular analysis of the choroideremia gene related clinical findings in two families with choroideremia.
    Lin Y, Liu X, Luo L, Qu B, Jiang S, Yang H, Liang X, Ye S, Liu Y.
    Mol Vis; 2011; 17():2564-9. PubMed ID: 22025891
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  • 22. Visual impairment and REP-1 gene mutations in Japanese choroideremia patients.
    Hayakawa M, Fujiki K, Hotta Y, Ito R, Ohki J, Ono J, Saito A, Nakayasu K, Kanai A, Ishidoh K, Kominami E, Yoshida K, Kim KC, Ohashi H.
    Ophthalmic Genet; 1999 Jun; 20(2):107-15. PubMed ID: 10420196
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  • 24. Copy number variant analysis in CHM to detect duplications underlying choroideremia.
    Chi JY, MacDonald IM, Hume S.
    Ophthalmic Genet; 2013 Dec; 34(4):229-33. PubMed ID: 23273018
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  • 29. Clinical characteristics of a large choroideremia pedigree carrying a novel CHM mutation.
    Huang AS, Kim LA, Fawzi AA.
    Arch Ophthalmol; 2012 Sep; 130(9):1184-9. PubMed ID: 22965595
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  • 31. Multimodal assessment of choroideremia patients defines pre-treatment characteristics.
    Seitz IP, Zhour A, Kohl S, Llavona P, Peter T, Wilhelm B, Zrenner E, Ueffing M, Bartz-Schmidt KU, Fischer MD.
    Graefes Arch Clin Exp Ophthalmol; 2015 Dec; 253(12):2143-50. PubMed ID: 25744334
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  • 34. New type of mutations in three spanish families with choroideremia.
    Garcia-Hoyos M, Lorda-Sanchez I, Gómez-Garre P, Villaverde C, Cantalapiedra D, Bustamante A, Diego-Alvarez D, Vallespin E, Gallego-Merlo J, Trujillo MJ, Ramos C, Ayuso C.
    Invest Ophthalmol Vis Sci; 2008 Apr; 49(4):1315-21. PubMed ID: 18385043
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  • 37. Large gene deletion and changes in corneal endothelial cells in a family with choroideremia.
    Lee SY, Yu WK, Lin PK.
    Invest Ophthalmol Vis Sci; 2015 Feb 26; 56(3):1887-93. PubMed ID: 25722215
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  • 38. [Clinical and genetic features of choroideremia].
    Ohba N, Isashiki Y.
    Nippon Ganka Gakkai Zasshi; 1999 Nov 26; 103(11):773-81. PubMed ID: 10589235
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