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Journal Abstract Search

419 related items for PubMed ID: 17557238

  • 1. [Study on clinical features and fluorescence in situ hybridization detections of 22q11 microdeletion syndrome].
    Qin YF, Yang JB, Xie CH, Shao J, Zhao ZY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):284-7. PubMed ID: 17557238
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  • 2. [Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome].
    Muñoz S, Garay F, Flores I, Heusser F, Talesnik E, Aracena M, Mellado C, Méndez C, Arnaiz P, Repetto G.
    Rev Med Chil; 2001 May; 129(5):515-21. PubMed ID: 11464533
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  • 7. Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies.
    Beauchesne LM, Warnes CA, Connolly HM, Ammash NM, Grogan M, Jalal SM, Michels VV.
    J Am Coll Cardiol; 2005 Feb 15; 45(4):595-8. PubMed ID: 15708709
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  • 13. Inherited t(9;22) as the cause of DiGeorge syndrome: a case report.
    Shuib S, Abdul Latif Z, Abidin NZ, Akmal SN, Zakaria Z.
    Malays J Pathol; 2009 Dec 15; 31(2):133-6. PubMed ID: 20514857
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