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Journal Abstract Search

108 related items for PubMed ID: 15389824

  • 1. Dysplastic changes in the peripheral blood of children with microdeletion 22q11.2.
    Ozbek N, Derbent M, Olcay L, Yilmaz Z, Tokel K.
    Am J Hematol; 2004 Oct; 77(2):126-31. PubMed ID: 15389824
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  • 2. 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; 24(3):349-71. PubMed ID: 15929620
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  • 3. [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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  • 6. Conotruncal heart defects: impact of genetic syndromes on immediate operative mortality.
    Anaclerio S, Di Ciommo V, Michielon G, Digilio MC, Formigari R, Picchio FM, Gargiulo G, Di Donato R, De Ioris MA, Marino B.
    Ital Heart J; 2004 Aug; 5(8):624-8. PubMed ID: 15554034
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  • 7. 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; 76(4):262-5. PubMed ID: 16575883
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  • 8. [Frequency of 22q11 deletions in children with isolated conotruncal defects].
    Shen L, Xu YJ, Zhao PJ, Sun K.
    Zhongguo Dang Dai Er Ke Za Zhi; 2009 Jan; 11(1):25-8. PubMed ID: 19149917
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  • 9. Genetic background of congenital conotruncal heart defects--a study of 45 families.
    Kwiatkowska J, Wierzba J, Aleszewicz-Baranowska J, Ereciński J.
    Kardiol Pol; 2007 Jan; 65(1):32-7; discussion 38-9. PubMed ID: 17295158
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  • 11. [22q11 microdeletion test in patients with congenital heart defects by quantitative fluorescent PCR].
    Chen Y, Mao J, Kwok KY, Kan HJ, Cheng HB, Li HB, Liu MJ, Sun Y, Yan WH, Li H, Choy KW.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Oct; 27(5):571-5. PubMed ID: 20931540
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  • 12. Myelodysplastic features in visceral leishmaniasis.
    Yarali N, Fişgin T, Duru F, Kara A.
    Am J Hematol; 2002 Nov; 71(3):191-5. PubMed ID: 12410574
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  • 13. 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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  • 14. Isochromosome of a deleted 20q: a rare but recurrent chromosome abnormality in myelodysplastic syndromes.
    Saunders K, Czepulkowski B, Sivalingam R, Hayes JP, Aldouri M, Sekhar M, Cummins M, Ho A, Mufti GJ.
    Cancer Genet Cytogenet; 2005 Jan 15; 156(2):154-7. PubMed ID: 15642396
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  • 18. Fluorescence in situ hybridization improves the detection of 5q31 deletion in myelodysplastic syndromes without cytogenetic evidence of 5q-.
    Mallo M, Arenillas L, Espinet B, Salido M, Hernández JM, Lumbreras E, del Rey M, Arranz E, Ramiro S, Font P, González O, Renedo M, Cervera J, Such E, Sanz GF, Luño E, Sanzo C, González M, Calasanz MJ, Mayans J, García-Ballesteros C, Amigo V, Collado R, Oliver I, Carbonell F, Bureo E, Insunza A, Yañez L, Muruzabal MJ, Gómez-Beltrán E, Andreu R, León P, Gómez V, Sanz A, Casasola N, Moreno E, Alegre A, Martín ML, Pedro C, Serrano S, Florensa L, Solé F.
    Haematologica; 2008 Jul 15; 93(7):1001-8. PubMed ID: 18591625
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  • 19. 20q- clonality in a case of oral sweet syndrome and myelodysplasia.
    Van Loon K, Gill RM, McMahon P, Chigurupati R, Siddiqi I, Fox L, Damon L, McCalmont TH, Jordan R, Wolf J.
    Am J Clin Pathol; 2012 Feb 15; 137(2):310-5. PubMed ID: 22261459
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  • 20. Allelic variations at the haploid TBX1 locus do not influence the cardiac phenotype in cases of 22q11 microdeletion.
    Voelckel MA, Girardot L, Giusiano B, Levy N, Philip N.
    Ann Genet; 2004 Feb 15; 47(3):235-40. PubMed ID: 15337468
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