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Journal Abstract Search

119 related items for PubMed ID: 8723074

  • 1. Exclusion of 22q11 deletion in Noonan syndrome with tetralogy of Fallot.
    Digilio MC, Marino B, Giannotti A, Dallapiccola B.
    Am J Med Genet; 1996 Apr 24; 62(4):413-4. PubMed ID: 8723074
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  • 3. Familial deletion of 22q11.2.
    Rodríguez Criado G, Gruesomontero J, Delicado Navarro A.
    Genet Couns; 1999 Apr 24; 10(3):325-7. PubMed ID: 10546107
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  • 7. Associated anomalies in asymmetric crying facies and 22q11 deletion.
    Akcakus M, Ozkul Y, Gunes T, Kurtoglu S, Cetin N, Kisaarslan AP, Dundar M.
    Genet Couns; 2003 Apr 24; 14(3):325-30. PubMed ID: 14577677
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  • 8. Asymmetric crying facies: a possible marker for congenital malformations.
    Rioja-Mazza D, Lieber E, Kamath V, Kalpatthi R.
    J Matern Fetal Neonatal Med; 2005 Oct 24; 18(4):275-7. PubMed ID: 16318980
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  • 9. 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 24; 76(4):262-5. PubMed ID: 16575883
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  • 11. Phenotypic discordance in monozygotic twins with 22q11.2 deletion.
    Yamagishi H, Ishii C, Maeda J, Kojima Y, Matsuoka R, Kimura M, Takao A, Momma K, Matsuo N.
    Am J Med Genet; 1998 Jul 24; 78(4):319-21. PubMed ID: 9714432
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  • 12. Frequency of 22q11.2 microdeletion in sporadic non-syndromic tetralogy of Fallot cases.
    Gioli-Pereira L, Pereira AC, Bergara D, Mesquita S, Lopes AA, Krieger JE.
    Int J Cardiol; 2008 Jun 06; 126(3):374-8. PubMed ID: 17604138
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  • 13. Smith-Magenis syndrome and tetralogy of Fallot.
    Sweeney E, Peart I, Tofeig M, Kerr B.
    J Med Genet; 1999 Jun 06; 36(6):501-2. PubMed ID: 10874646
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  • 15. 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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  • 17. Tetralogy of Fallot associated with chromosome 22q11 deletion.
    Momma K, Kondo C, Ando M, Matsuoka R, Takao A.
    Am J Cardiol; 1995 Sep 15; 76(8):618-21. PubMed ID: 7677092
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  • 20. 22q11.2 deletion status and disease burden in children and adolescents with tetralogy of Fallot.
    Mercer-Rosa L, Paridon SM, Fogel MA, Rychik J, Tanel RE, Zhao H, Zhang X, Yang W, Shults J, Goldmuntz E.
    Circ Cardiovasc Genet; 2015 Feb 15; 8(1):74-81. PubMed ID: 25561045
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