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Journal Abstract Search

565 related items for PubMed ID: 9986884

  • 1. Aortic arch anomalies associated with chromosome 22q11 deletion (CATCH 22).
    Momma K, Matsuoka R, Takao A.
    Pediatr Cardiol; 1999; 20(2):97-102. PubMed ID: 9986884
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  • 2. Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion.
    Momma K, Kondo C, Matsuoka R.
    J Am Coll Cardiol; 1996 Jan; 27(1):198-202. PubMed ID: 8522695
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  • 3. Laterality of the aortic arch and anomalies of the subclavian artery-reliable indicators for 22q11.2 deletion syndromes?
    Rauch R, Rauch A, Koch A, Zink S, Kaulitz R, Girisch M, Singer H, Hofbeck M.
    Eur J Pediatr; 2004 Nov; 163(11):642-5. PubMed ID: 15300432
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  • 4. Frequency of 22q11 deletions in patients with conotruncal defects.
    Goldmuntz E, Clark BJ, Mitchell LE, Jawad AF, Cuneo BF, Reed L, McDonald-McGinn D, Chien P, Feuer J, Zackai EH, Emanuel BS, Driscoll DA.
    J Am Coll Cardiol; 1998 Aug; 32(2):492-8. PubMed ID: 9708481
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  • 5. 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 Aug; 3(1):45-8. PubMed ID: 11339377
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  • 10. Hypoparathyroidism in conotruncal heart defects.
    Koch A, Hofbeck M, Buheitel G, Dörr HG, Rauch A, Rauch R, Singer H.
    Eur J Pediatr; 2002 Apr; 161(4):208-11. PubMed ID: 12014387
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  • 12. Chromosome 22q11 deletions in patients with conotruncal heart defects.
    Khositseth A, Tocharoentanaphol C, Khowsathit P, Ruangdaraganon N.
    Pediatr Cardiol; 2005 Apr; 26(5):570-3. PubMed ID: 16132309
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  • 13. [22q11 deletion in conotruncal anomalies].
    Kádár K.
    Orv Hetil; 2005 Feb 20; 146(8):363-6. PubMed ID: 15803887
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  • 14. Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome.
    Momma K, Kondo C, Matsuoka R, Takao A.
    Am J Cardiol; 1996 Sep 01; 78(5):591-4. PubMed ID: 8806353
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  • 15. 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 01; 105(4):284-9. PubMed ID: 16618608
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  • 16. 22q11.2 deletion syndrome and congenital heart disease.
    Goldmuntz E.
    Am J Med Genet C Semin Med Genet; 2020 Mar 01; 184(1):64-72. PubMed ID: 32049433
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  • 19. 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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  • 20. 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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