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Journal Abstract Search

180 related items for PubMed ID: 22456069

  • 1. [Analysis of prenatal diagnosis for seven high-risk fetuses with Wiskott-Aldrich syndrome].
    Zhao Q, Zhang ZY, Zhao XD, Jiang LP, Zhao Y, Yang XQ.
    Zhonghua Er Ke Za Zhi; 2012 Jan; 50(1):15-9. PubMed ID: 22456069
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  • 2. [Mutation analysis of WASP gene and prenatal diagnosis of Wiskott-Aldrich syndrome].
    Liu N, Shi H, Kong X, Wu Q, Xu X, Bai Q, Feng Y, Zhao Z.
    Zhonghua Er Ke Za Zhi; 2014 Sep; 52(9):662-6. PubMed ID: 25476427
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  • 3. [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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  • 4. Analysis of clinical and molecular characteristics of Wiskott-Aldrich syndrome in 24 patients from 23 unrelated Chinese families.
    Zhang ZY, Xiao HQ, Jiang LP, Zhou Y, Zhao Q, Yu J, Liu W, Yang XQ, Zhao XD.
    Pediatr Allergy Immunol; 2010 May; 21(3):522-32. PubMed ID: 20546529
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  • 5. Wiskott-Aldrich syndrome/X-linked thrombocytopenia in China: Clinical characteristic and genotype-phenotype correlation.
    Liu DW, Zhang ZY, Zhao Q, Jiang LP, Liu W, Tu WW, Song WX, Zhao XD.
    Pediatr Blood Cancer; 2015 Sep; 62(9):1601-8. PubMed ID: 25931402
    [Abstract] [Full Text] [Related]

  • 6. Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis.
    Giliani S, Fiorini M, Mella P, Candotti F, Schumacher RF, Wengler GS, Lalatta F, Fasth A, Badolato R, Ugazio AG, Albertini A, Notarangelo LD.
    Prenat Diagn; 1999 Jan; 19(1):36-40. PubMed ID: 10073904
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  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. WASP-WIP complex in the molecular pathogenesis of Wiskott-Aldrich syndrome.
    Sasahara Y.
    Pediatr Int; 2016 Jan; 58(1):4-7. PubMed ID: 26331277
    [Abstract] [Full Text] [Related]

  • 9. Molecular diagnosis of Wiskott-Aldrich syndrome in Taiwan.
    Chien YH, Hwu WL, Ariga T, Chang KW, Yang YH, Lin KH, Chiang BL.
    J Microbiol Immunol Infect; 2004 Oct; 37(5):276-81. PubMed ID: 15497008
    [Abstract] [Full Text] [Related]

  • 10. Mutation spectrum in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia: identification of twelve different mutations in the WASP gene.
    Schwartz M, Békássy A, Donnér M, Hertel T, Hreidarson S, Kerndrup G, Stormorken H, Stokland T, Tranebjaerg L, Orstavik KH, Skovby F.
    Thromb Haemost; 1996 Apr; 75(4):546-50. PubMed ID: 8743175
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  • 15. Wiskott-Aldrich syndrome in a girl caused by heterozygous WASP mutation and extremely skewed X-chromosome inactivation: a novel association with maternal uniparental isodisomy 6.
    Takimoto T, Takada H, Ishimura M, Kirino M, Hata K, Ohara O, Morio T, Hara T.
    Neonatology; 2015 Apr; 107(3):185-90. PubMed ID: 25633059
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  • 17. False-negative prenatal exclusion of Wiskott-Aldrich syndrome by measurement of fetal platelet count and size.
    Lorenz P, Bollmann R, Hinkel GK, Mächler M, Siegert G, Stamminger G, Wendisch J, Ziemer S.
    Prenat Diagn; 1991 Nov; 11(11):819-25. PubMed ID: 1754554
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  • 18. Effects of Wiskott-Aldrich Syndrome Protein Deficiency on IL-10-Producing Regulatory B Cells in Humans and Mice.
    Du HQ, Zhang X, An YF, Ding Y, Zhao XD.
    Scand J Immunol; 2015 Jun; 81(6):483-93. PubMed ID: 25728049
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  • 20. Characterization of a deletion mutation involving exons 3-7 of the WASP gene detected in a patient with Wiskott-Aldrich syndrome.
    Ariga T, Yamada M, Ito S, Iwamura M, Iseki M, Sakiyama Y.
    Hum Mutat; 1997 Jun; 10(4):310-6. PubMed ID: 9338585
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