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Journal Abstract Search

256 related items for PubMed ID: 22088244

  • 1. [Relationship between 22q11 microdeletion syndrome and congenital heart disease].
    Qin YF, Xie CH, Yang JB, Wu DW, Shao J, Zhao ZY.
    Zhonghua Xin Xue Guan Bing Za Zhi; 2011 Jul; 39(7):631-5. PubMed ID: 22088244
    [Abstract] [Full Text] [Related]

  • 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. 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. [Analysis of microdeletions in 22q11 in Colombian patients with congenital heart disease].
    Salazar M, Villalba G, Mateus H, Villegas V, Fonseca D, Núñez F, Caicedo V, Pachón S, Bernal JE.
    Invest Clin; 2011 Dec 15; 52(4):334-43. PubMed ID: 22523843
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  • 8. Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations.
    Alikaşifoğlu M, Malkoç N, Ceviz N, Ozme S, Uludoğan S, Tunçbilek E.
    Turk J Pediatr; 2000 Dec 15; 42(3):215-8. PubMed ID: 11105620
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  • 10. [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 15; 129(5):515-21. PubMed ID: 11464533
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  • 12. Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion.
    Momma K, Kondo C, Matsuoka R.
    J Am Coll Cardiol; 1996 Jan 15; 27(1):198-202. PubMed ID: 8522695
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  • 14. Microdeletion 22q11 and oesophageal atresia.
    Digilio MC, Marino B, Bagolan P, Giannotti A, Dallapiccola B.
    J Med Genet; 1999 Feb 15; 36(2):137-9. PubMed ID: 10051013
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  • 15. [Microdeletion of 22q11 and conotruncal cardiopathies: contribution of prenatal diagnosis].
    Verspyck E, Joly G, Rossi A, David N, Blaysat G, Henocq A, Moirot H, Labadie G, Marpeau L.
    J Gynecol Obstet Biol Reprod (Paris); 1999 Oct 15; 28(6):534-7. PubMed ID: 10598346
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  • 18. Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland.
    Wozniak A, Wolnik-Brzozowska D, Wisniewska M, Glazar R, Materna-Kiryluk A, Moszura T, Badura-Stronka M, Skolozdrzy J, Krawczynski MR, Zeyland J, Bobkowski W, Slomski R, Latos-Bielenska A, Siwinska A.
    BMC Pediatr; 2010 Dec 06; 10():88. PubMed ID: 21134246
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  • 19. Mosaic 22q11.2 deletion and tetralogy of Fallot with absent pulmonary valve: an unreported association.
    Prabhu S, Jenny B, James H, Provenzano S.
    World J Pediatr Congenit Heart Surg; 2015 Apr 06; 6(2):342-5. PubMed ID: 25870364
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