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Journal Abstract Search

345 related items for PubMed ID: 21390462

  • 1. [22q11.2 deletion syndrome and complex congenital heart defects].
    Rosa RF, Trevisan P, Koshiyama DB, Pilla CB, Zen PR, Varella-Garcia M, Paskulin GA.
    Rev Assoc Med Bras (1992); 2011; 57(1):62-5. PubMed ID: 21390462
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  • 4. CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects.
    Hou JW, Wang JK, Tsai WY, Chou CC, Wang TR.
    J Formos Med Assoc; 1997 Jun; 96(6):419-23. PubMed ID: 9216164
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  • 6. 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; 157(11):881-4. PubMed ID: 9835429
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  • 10. The 22q11.2 Deletion Syndrome in Congenital Heart Defects: Prevalence of Microdeletion Syndrome in Cameroon.
    Wonkam A, Toko R, Chelo D, Tekendo-Ngongang C, Kingue S, Dahoun S.
    Glob Heart; 2017 Jun; 12(2):115-120. PubMed ID: 28302550
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  • 11. Microdeletion 22q11 and oesophageal atresia.
    Digilio MC, Marino B, Bagolan P, Giannotti A, Dallapiccola B.
    J Med Genet; 1999 Feb; 36(2):137-9. PubMed ID: 10051013
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  • 14. 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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  • 17. [Study on the relationship between 22q11 microdeletion and congenital heart disease].
    Du YR, Yang HJ, Tan Z, Huang Y, Li SL, Tian JW, Zhang GY, Li P, Fu SB.
    Yi Chuan; 2005 Nov; 27(6):873-6. PubMed ID: 16378931
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  • 19. 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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