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Journal Abstract Search

140 related items for PubMed ID: 11954747

  • 1. Ventricular septal defect and deletion of chromosome 22q11: anatomical types and aortic arch anomalies.
    Toscano A, Anaclerio S, Digilio MC, Giannotti A, Fariello G, Dallapiccola B, Marino B.
    Eur J Pediatr; 2002 Feb; 161(2):116-7. PubMed ID: 11954747
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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 Feb; 3(1):45-8. PubMed ID: 11339377
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  • 3. Interruption of the aortic arch associated with deletion of chromosome 22q11 is associated with a subarterial and doubly committed ventricular septal defect in Japanese patients.
    Momma K, Ando M, Matsuoka R, Joo K.
    Cardiol Young; 1999 Sep; 9(5):463-7. PubMed ID: 10535824
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  • 4. The genetic implication for preceding generations of the prenatal diagnosis of interrupted aortic arch in association with unsuspected DiGeorge anomaly.
    Puder KS, Humes RA, Gold RL, Bawle EV, Goyert GL.
    Am J Obstet Gynecol; 1995 Jul; 173(1):239-41. PubMed ID: 7631695
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  • 5. 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; 9(5):516-8. PubMed ID: 10535835
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  • 6. A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma.
    Tarlan B, Kiratli H, Kılıç E, Utine E, Boduroğlu K.
    Ophthalmic Genet; 2014 Dec; 35(4):248-51. PubMed ID: 23834556
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  • 8. Aortic arch anomalies associated with chromosome 22q11 deletion (CATCH 22).
    Momma K, Matsuoka R, Takao A.
    Pediatr Cardiol; 1999 Dec; 20(2):97-102. PubMed ID: 9986884
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  • 10. DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin.
    Wilson DI, Cross IE, Goodship JA, Coulthard S, Carey AH, Scambler PJ, Bain HH, Hunter AS, Carter PE, Burn J.
    Br Heart J; 1991 Oct; 66(4):308-12. PubMed ID: 1747284
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  • 11. 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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  • 12. Cervical aortic arch and Kommerell's diverticulum associated with the anomalous subaortic left brachiocephalic vein in a patient with chromosome 22q11.2 deletion.
    Nagashima M, Shikata F, Higaki T, Kawachi K.
    Interact Cardiovasc Thorac Surg; 2010 Aug; 11(2):202-3. PubMed ID: 20472649
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  • 15. Interrupted right aortic arch and origin of the left pulmonary artery from the aorta in DiGeorge syndrome.
    Sett SS, Sandor GG, Mawson JB.
    Cardiol Young; 2001 Nov; 11(6):676-9. PubMed ID: 11813925
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  • 16. 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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  • 17. A new embryonic linkage between chromosome 22q11 deletion and a right ductus from a right aortic arch in a neonate with DiGeorge syndrome.
    Lee ML, Chaou WT, Wang YM, Fang W, Chiu IS.
    Int J Cardiol; 2001 Jul; 79(2-3):315-6. PubMed ID: 11488286
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  • 20. Outcomes using predominantly single-stage approach to interrupted aortic arch and associated defects.
    Flint JD, Gentles TL, MacCormick J, Spinetto H, Finucane AK.
    Ann Thorac Surg; 2010 Feb; 89(2):564-9. PubMed ID: 20103342
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