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525 related items for PubMed ID: 8757559

  • 1. Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: a three-year prospective study.
    Webber SA, Hatchwell E, Barber JC, Daubeney PE, Crolla JA, Salmon AP, Keeton BR, Temple IK, Dennis NR.
    J Pediatr; 1996 Jul; 129(1):26-32. PubMed ID: 8757559
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  • 2. Anatomic patterns of conotruncal defects associated with deletion 22q11.
    Marino B, Digilio MC, Toscano A, Anaclerio S, Giannotti A, Feltri C, de Ioris MA, Angioni A, Dallapiccola B.
    Genet Med; 2001 Jul; 3(1):45-8. PubMed ID: 11339377
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  • 3. [Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2].
    Trost D, Engels H, Bauriedel G, Wiebe W, Schwanitz G.
    Dtsch Med Wochenschr; 1999 Jan 08; 124(1-2):3-7. PubMed ID: 9951451
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  • 5. Chromosome 22q11 deletions in patients with conotruncal heart defects.
    Khositseth A, Tocharoentanaphol C, Khowsathit P, Ruangdaraganon N.
    Pediatr Cardiol; 2005 Jan 08; 26(5):570-3. PubMed ID: 16132309
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  • 13. 22q11.2 deletion detected by in situ hybridization in Mexican patients with velocardiofacial syndrome-like features.
    Ramírez-Velazco A, Rivera H, Vásquez-Velázquez AI, Aguayo-Orozco TA, Delgadillo-Pérez S, Domínguez MG.
    Colomb Med (Cali); 2018 Sep 30; 49(3):219-222. PubMed ID: 30410196
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  • 14. 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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  • 15. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.
    Sergi C, Serpi M, Müller-Navia J, Schnabel PA, Hagl S, Otto HF, Ulmer HE.
    Pathologica; 1999 Jun 15; 91(3):166-72. PubMed ID: 10536461
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  • 16. Persistent fifth aortic arch associated with 22q11.2 deletion syndrome.
    Lee ML, Chen HN, Chen M, Tsao LY, Wang BT, Lee MH, Chiu IS.
    J Formos Med Assoc; 2006 Apr 15; 105(4):284-9. PubMed ID: 16618608
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  • 19. Interruption of the aortic arch at the isthmus with DiGeorge syndrome and 22q11.2 deletion.
    Takahashi K, Kuwahara T, Nagatsu M.
    Cardiol Young; 1999 Sep 15; 9(5):516-8. PubMed ID: 10535835
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  • 20. Aortic arch anomalies associated with chromosome 22q11 deletion (CATCH 22).
    Momma K, Matsuoka R, Takao A.
    Pediatr Cardiol; 1999 Sep 15; 20(2):97-102. PubMed ID: 9986884
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