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Journal Abstract Search

817 related items for PubMed ID: 18636635

  • 1. Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome.
    Carotti A, Digilio MC, Piacentini G, Saffirio C, Di Donato RM, Marino B.
    Dev Disabil Res Rev; 2008; 14(1):35-42. PubMed ID: 18636635
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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. DiGeorge syndrome: new insights.
    Goldmuntz E.
    Clin Perinatol; 2005 Dec; 32(4):963-78, ix-x. PubMed ID: 16325672
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  • 4. 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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  • 6. Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11.
    Marino B, Digilio MC, Toscano A, Giannotti A, Dallapiccola B.
    Genet Couns; 1999 Aug; 10(1):25-33. PubMed ID: 10191426
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  • 7. Pulmonary atresia with ventricular septal defect: prevalence of deletion 22q11 in the different anatomic patterns.
    Anaclerio S, Marino B, Carotti A, Digilio MC, Toscano A, Gitto P, Giannotti A, Di Donato R, Dallapiccola B.
    Ital Heart J; 2001 May; 2(5):384-7. PubMed ID: 11392644
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  • 8. 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; 91(3):166-72. PubMed ID: 10536461
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  • 10. Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: a 6-year prospective study.
    Boudjemline Y, Fermont L, Le Bidois J, Lyonnet S, Sidi D, Bonnet D.
    J Pediatr; 2001 Apr; 138(4):520-4. PubMed ID: 11295715
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  • 14. 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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  • 16. Chromosome 22q11 deletions in patients with selected outflow tract malformations.
    Frohn-Mulder IM, Wesby Swaay E, Bouwhuis C, Van Hemel JO, Gerritsma E, Niermeyer MF, Hess J.
    Genet Couns; 1999 Aug; 10(1):35-41. PubMed ID: 10191427
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  • 18. Cardiovascular anomalies in patients with chromosome 22q11.2 deletion: a Korean multicenter study.
    Park IS, Ko JK, Kim YH, Yoo HW, Seo EJ, Choi JY, Gil HY, Kim SJ.
    Int J Cardiol; 2007 Jan 08; 114(2):230-5. PubMed ID: 16824627
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  • 19. Aortic arch anomalies associated with chromosome 22q11 deletion (CATCH 22).
    Momma K, Matsuoka R, Takao A.
    Pediatr Cardiol; 1999 Jan 08; 20(2):97-102. PubMed ID: 9986884
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  • 20. Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies.
    Iserin L, de Lonlay P, Viot G, Sidi D, Kachaner J, Munnich A, Lyonnet S, Vekemans M, Bonnet D.
    Eur J Pediatr; 1998 Nov 08; 157(11):881-4. PubMed ID: 9835429
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