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Journal Abstract Search

525 related items for PubMed ID: 8757559

  • 21. 22q11 deletions in fetuses with malformations of the outflow tracts or interruption of the aortic arch: impact of additional ultrasound signs.
    Volpe P, Marasini M, Caruso G, Marzullo A, Buonadonna AL, Arciprete P, Di Paolo S, Volpe G, Gentile M.
    Prenat Diagn; 2003 Sep; 23(9):752-7. PubMed ID: 12975788
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  • 31. Variation in prevalence of chromosome 22q11 deletion in subtypes of conotruncal defect in 254 children.
    Anilkumar A, Kappanayil M, Thampi MV, Nampoothiri S, Sundaram KR, Vasudevan DM.
    Acta Paediatr; 2011 Sep; 100(9):e97-100. PubMed ID: 21418101
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  • 33. Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.
    Goldmuntz E, Driscoll D, Budarf ML, Zackai EH, McDonald-McGinn DM, Biegel JA, Emanuel BS.
    J Med Genet; 1993 Oct; 30(10):807-12. PubMed ID: 7901419
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  • 34. 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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  • 35. 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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