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Journal Abstract Search

139 related items for PubMed ID: 17107413

  • 1. New mutations of KIT gene in two Chinese patients with piebaldism.
    Lin ZM, Xu Z, Bu DF, Yang Y.
    Br J Dermatol; 2006 Dec; 155(6):1303-4. PubMed ID: 17107413
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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; 20(3):234. PubMed ID: 12204004
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  • 3. 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; 35(1):29-33. PubMed ID: 15194144
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  • 6. [A novel KIT gene mutation from a family with piebaldism in the southern part of China].
    Deng WP, Huang YS, Lu C, Lan W, Zhu GX, Lin QD, Feng PY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):668-70. PubMed ID: 16331568
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  • 9. A 12-bp deletion (7818del12) in the c-kit protooncogene in a large Italian kindred with piebaldism.
    Riva P, Milani N, Gandolfi P, Larizza L.
    Hum Mutat; 1995 Dec; 6(4):343-5. PubMed ID: 8680409
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  • 10. [Mastocytosis or piebaldism--the KIT mutation decides].
    Roupe G.
    Lakartidningen; 2004 Mar 11; 101(11):1008-9. PubMed ID: 15055122
    [No Abstract] [Full Text] [Related]

  • 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 Mar 11; 21(3):446-7. PubMed ID: 21680281
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  • 12. Molecular characterization of two novel KIT mutations in patients with piebaldism.
    Wasag B, Chmara M, Legius E.
    J Dermatol Sci; 2012 Apr 11; 66(1):78-9. PubMed ID: 22264755
    [No Abstract] [Full Text] [Related]

  • 13. Repigmentation of leukoderma in a piebald patient associated with a novel c-KIT gene mutation, G592E, of the tyrosine kinase domain.
    Arase N, Wataya-Kaneda M, Oiso N, Tanemura A, Kawada A, Suzuki T, Katayama I.
    J Dermatol Sci; 2011 Nov 11; 64(2):147-9. PubMed ID: 21925843
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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 11; 111(2):337-8. PubMed ID: 9699740
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  • 17. A Japanese piebald patient with auburn hair colour associated with a novel mutation p.P832L in the KIT gene and a homozygous variant p.I120T in the MC1R gene.
    Oiso N, Kishida K, Fukai K, Motokawa T, Hosomi N, Suzuki T, Mitsuhashi Y, Tsuboi R, Kawada A.
    Br J Dermatol; 2009 Aug 11; 161(2):468-9. PubMed ID: 19416250
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  • 18. 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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  • 20. A novel mutation of KIT gene results in piebaldism in a Chinese family.
    Xu XH, Ma L, Weng L, Xing H.
    J Eur Acad Dermatol Venereol; 2016 Feb 06; 30(2):336-8. PubMed ID: 25199540
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