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Journal Abstract Search

139 related items for PubMed ID: 11074500

  • 1. Three novel mutations of the proto-oncogene KIT cause human piebaldism.
    Syrris P, Malik NM, Murday VA, Patton MA, Carter ND, Hughes HE, Metcalfe K.
    Am J Med Genet; 2000 Nov 06; 95(1):79-81. PubMed ID: 11074500
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  • 2. Human piebaldism: six novel mutations of the proto-oncogene KIT.
    Syrris P, Heathcote K, Carrozzo R, Devriendt K, Elçioglu N, Garrett C, McEntagart M, Carter ND.
    Hum Mutat; 2002 Sep 06; 20(3):234. PubMed ID: 12204004
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  • 3. A novel KIT missense mutation in one Chinese family with piebaldism.
    Yin XY, Ren YQ, Yang S, Xu SX, Zhou FS, Du WH, Lin D, Wang PG, Zhang SM, Zhang XJ.
    Arch Dermatol Res; 2009 Jun 06; 301(5):387-9. PubMed ID: 19430803
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  • 7. Piebaldism and neurofibromatosis type 1: family report.
    Duarte AF, Mota A, Baudrier T, Morais P, Santos A, Cerqueira R, Tavares P, Azevedo F.
    Dermatol Online J; 2010 Jan 15; 16(1):11. PubMed ID: 20137753
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  • 11. Two children with a mild or moderate piebaldism phenotype and a father without leukoderma in a family with the same recurrent missense mutation in the kinase domain of KIT.
    Narita T, Oiso N, Fukai K, Motokawa T, Hayashi M, Yokoyama K, Hozumi Y, Kawada A, Suzuki T.
    Eur J Dermatol; 2011 Jan 15; 21(3):446-7. PubMed ID: 21680281
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  • 12. A novel mutation of the KIT gene in a Chinese family with piebaldism.
    Wen GD, Zhou C, Yu C, DU J, Xu QX, Liu ZY, Zhang JZ.
    Chin Med J (Engl); 2013 Jun 15; 126(12):2325-8. PubMed ID: 23786947
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  • 13. New KIT mutations in patients with piebaldism.
    Murakami T, Fukai K, Oiso N, Hosomi N, Kato A, Garganta C, Barnicoat A, Poppelaars F, Aquaron R, Paller AS, Ishii M.
    J Dermatol Sci; 2004 Jun 15; 35(1):29-33. PubMed ID: 15194144
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  • 14. Mutations in the ligand-binding domain of the kit receptor: an uncommon site in human piebaldism.
    Fleischman RA, Gallardo T, Mi X.
    J Invest Dermatol; 1996 Nov 15; 107(5):703-6. PubMed ID: 8875953
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  • 15. New mutations of KIT gene in two Chinese patients with piebaldism.
    Lin ZM, Xu Z, Bu DF, Yang Y.
    Br J Dermatol; 2006 Dec 15; 155(6):1303-4. PubMed ID: 17107413
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  • 16. A novel KIT gene missense mutation in a Japanese family with piebaldism.
    Nomura K, Hatayama I, Narita T, Kaneko T, Shiraishi M.
    J Invest Dermatol; 1998 Aug 15; 111(2):337-8. PubMed ID: 9699740
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