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200 related items for PubMed ID: 15099357

  • 1. Refined localization of dyschromatosis symmetrica hereditaria gene to a 9.4-cM region at 1q21-22 and a literature review of 136 cases reported in China.
    He PP, He CD, Cui Y, Yang S, Xu HH, Li M, Yuan WT, Gao M, Liang YH, Li CR, Xu SJ, Chen JJ, Chen HD, Huang W, Zhang XJ.
    Br J Dermatol; 2004 Apr; 150(4):633-9. PubMed ID: 15099357
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  • 6. Exclusion of linkage between dyschromatosis symmetrica hereditaria and chromosome 9.
    Kono M, Miyamura Y, Matsunaga J, Tomita Y.
    J Dermatol Sci; 2000 Feb; 22(2):88-95. PubMed ID: 10674821
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  • 7. A novel missense mutation in DSRAD in a family with dyschromatosis symmetrica hereditaria.
    Li M, Yang LJ, Shi YX, Huang HY.
    Arch Dermatol Res; 2007 Aug; 299(5-6):273-5. PubMed ID: 17569068
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  • 9. A novel insertion mutation in the ADAR1 gene of a Chinese family with dyschromatosis symmetrica hereditaria.
    Zhu CY, Zhu KJ, Zhou Y, Fan YM.
    Genet Mol Res; 2013 Aug 12; 12(3):2858-62. PubMed ID: 24065641
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  • 10. A new mutation of the double-stranded RNA-specific adenosine deaminase gene in a family with dyschromatosis symmetrica hereditaria.
    Liu Y, Xiao S, Peng Z, Chu Y, Wang J, Li X, Zhou S.
    Dermatology; 2006 Aug 12; 213(3):200-3. PubMed ID: 17033168
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  • 11. Hyper- and hypopigmented macules over palms and soles since birth--a case of dyschromatosis symmetrica hereditaria.
    Hemmati I, Lam J.
    Dermatol Online J; 2009 Nov 15; 15(11):5. PubMed ID: 19951641
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  • 12. Identification of two novel mutations in Chinese patients with Dyschromatosis symmetrica hereditaria.
    Li M, Li C, Hua H, Zhu W, Lu Y, Yang L.
    Arch Dermatol Res; 2005 Nov 15; 297(5):196-200. PubMed ID: 16215765
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  • 15. Dyschromatosis symmetrica hereditaria associated with neurological disorders.
    Kondo T, Suzuki T, Ito S, Kono M, Negoro T, Tomita Y.
    J Dermatol; 2008 Oct 15; 35(10):662-6. PubMed ID: 19017046
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  • 18. Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases.
    Oyama M, Shimizu H, Ohata Y, Tajima S, Nishikawa T.
    Br J Dermatol; 1999 Mar 15; 140(3):491-6. PubMed ID: 10233273
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  • 20. Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria: histological observation and comparison of genotypes and clinical phenotypes.
    Kondo T, Suzuki T, Mitsuhashi Y, Ito S, Kono M, Komine M, Akita H, Tomita Y.
    J Dermatol; 2008 Jul 15; 35(7):395-406. PubMed ID: 18705826
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