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Journal Abstract Search

78 related items for PubMed ID: 9988879

  • 1. Increased incidence of renal anomalies in patients with chromosome 22q11 microdeletion.
    Stewart TL, Irons MB, Cowan JM, Bianchi DW.
    Teratology; 1999 Jan; 59(1):20-2. PubMed ID: 9988879
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  • 3. 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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  • 6. 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 Feb 15; 14(3):325-30. PubMed ID: 14577677
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  • 8. 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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  • 10. Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci.
    Berend SA, Spikes AS, Kashork CD, Wu JM, Daw SC, Scambler PJ, Shaffer LG.
    Am J Med Genet; 2000 Apr 10; 91(4):313-7. PubMed ID: 10766989
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  • 12. DiGeorge syndrome: new insights.
    Goldmuntz E.
    Clin Perinatol; 2005 Dec 10; 32(4):963-78, ix-x. PubMed ID: 16325672
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  • 13. [Phenotypic variability of deletion 22q11.2. An analysis of 16 observations with special emphasis on the neurological manifestations].
    Eirís-Puñal J, Iglesias-Meleiro JM, Blanco-Barca MO, Fuster-Siebert M, Barros-Angueira F, Ansede A, Castro-Gago M.
    Rev Neurol; 2005 Dec 10; 37(7):601-7. PubMed ID: 14582013
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  • 17. Chromosome 22q11 deletion syndrome: the first three cases reported in Thailand.
    Ruangdaraganon N, Tocharoentanaphol C, Khowsathit P, Sombuntham T, Pongpanich B.
    J Med Assoc Thai; 1999 Nov 10; 82 Suppl 1():S179-85. PubMed ID: 10730540
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  • 20. [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 10; 23(3):250-5. PubMed ID: 16767657
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