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Journal Abstract Search

153 related items for PubMed ID: 10932799

  • 1. [Chromosome 22 (22q.11.2) deletion. Etiology of conotruncal heart abnormalities].
    Buendía Hernández A, Calderón-Colmenero J, Aizpuru E, Attie CL, Zabal C, Patiño E, Miranda I, Juanico A, Attie F.
    Arch Inst Cardiol Mex; 2000; 70(2):148-53. PubMed ID: 10932799
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  • 4. 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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  • 7. Congenital heart defects and chromosomal anomalies including 22q11 microdeletion (CATCH 22).
    Soares G, Alvares S, Rocha C, Teixeira MF, Mota MC, Reis MI, Feijó MJ, Lima MR, Pinto MR.
    Rev Port Cardiol; 2005 Mar 15; 24(3):349-71. PubMed ID: 15929620
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  • 8. 22q11.2 deletion mosaicism in patients with conotruncal heart defects.
    Jianrong L, Yinglong L, Xiaodong L, Cuntao Y, Bin C, Bo W.
    Birth Defects Res A Clin Mol Teratol; 2006 Apr 15; 76(4):262-5. PubMed ID: 16575883
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  • 17. Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations.
    Alikaşifoğlu M, Malkoç N, Ceviz N, Ozme S, Uludoğan S, Tunçbilek E.
    Turk J Pediatr; 2000 Apr 15; 42(3):215-8. PubMed ID: 11105620
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  • 18. [Detection and related analysis to chromosome 22q11 microdeletion in patients with congenital heart diseases].
    Xu ZF, Yi L, Mo XM, Hu Y, Wang DJ, Zhu RF, Jiang YZ, Wu X, Wu Z, Shen L, Zhang Y, Zhong XL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun 15; 23(3):250-5. PubMed ID: 16767657
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  • 20. San Luis Valley recombinant chromosome 8 and tetralogy of Fallot: a review of chromosome 8 anomalies and congenital heart disease.
    Gelb BD, Towbin JA, McCabe ER, Sujansky E.
    Am J Med Genet; 1991 Sep 15; 40(4):471-6. PubMed ID: 1746613
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