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Journal Abstract Search

435 related items for PubMed ID: 23264413

  • 1. Detection of six novel mutations in WASP gene in fifteen Iranian Wiskott-Aldrich patients.
    Safaei S, Fazlollahi MR, Houshmand M, Hamidieh AA, Bemanian MH, Alavi S, Mousavi F, Pourpak Z, Moin M.
    Iran J Allergy Asthma Immunol; 2012 Dec; 11(4):345-8. PubMed ID: 23264413
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  • 2. Wiskott-Aldrich syndrome in Argentina: 17 unique, including nine novel, mutations.
    El-Hakeh J, Rosenzweig S, Oleastro M, Basack N, Berozdnik L, Molina F, Rivas EM, Zelazko M, Danielian S.
    Hum Mutat; 2002 Feb; 19(2):186-7. PubMed ID: 11793485
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  • 5. Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR.
    Proust A, Guillet B, Picard C, de Saint Basile G, Pondarré C, Tamary H, Dreyfus M, Tchernia G, Fischer A, Delaunay J.
    Blood Cells Mol Dis; 2007 Feb; 39(1):102-6. PubMed ID: 17400488
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  • 6. [Identification of two novel WASP gene mutations in 3 boys with Wiskott-Aldrich syndrome].
    Jiang LP, Xu YH, Yang XQ, Liu EM, Wang LJ, Lau YL, Chan KW.
    Zhonghua Er Ke Za Zhi; 2003 Aug; 41(8):590-3. PubMed ID: 14744380
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  • 8. Identification of WASP mutations in 10 Australian families with Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
    Bourne HC, Weston S, Prasad M, Edkins E, Benson EM.
    Pathology; 2004 Jun; 36(3):262-4. PubMed ID: 15203732
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  • 9. Novel mutations in the Wiskott-Aldrich syndrome protein gene and their effects on transcriptional, translational, and clinical phenotypes.
    Lemahieu V, Gastier JM, Francke U.
    Hum Mutat; 1999 Jun; 14(1):54-66. PubMed ID: 10447259
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  • 10. Clinical and molecular characterization of Thai patients with Wiskott-Aldrich syndrome.
    Amarinthnukrowh P, Ittiporn S, Tongkobpetch S, Chatchatee P, Sosothikul D, Shotelersuk V, Suphapeetiporn K.
    Scand J Immunol; 2013 Jan; 77(1):69-74. PubMed ID: 23033889
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  • 13. A case of Wiskott-Aldrich syndrome with de novo mutation at exon 4.
    Doğu F, Ariga T, Ikincioğullari A, Bozdoğan G, Aytekin C, Metin A, Babacan E.
    Turk J Pediatr; 2006 Jan; 48(1):66-8. PubMed ID: 16562789
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  • 18. [Analysis of clinical features and gene mutations in 6 patients with Wiskott-Aldrich syndrome].
    Jiang MH, Wang ZY, Su J, Cao LJ, Li JQ, Sun XH, Bai X, Wang GF, Ruan CG.
    Zhonghua Xue Ye Xue Za Zhi; 2011 Sep; 32(9):577-82. PubMed ID: 22338148
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