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Journal Abstract Search

171 related items for PubMed ID: 12494430

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  • 3. 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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  • 7. Chromosomal abnormalities among children born with conotruncal cardiac defects.
    Lammer EJ, Chak JS, Iovannisci DM, Schultz K, Osoegawa K, Yang W, Carmichael SL, Shaw GM.
    Birth Defects Res A Clin Mol Teratol; 2009 Jan; 85(1):30-5. PubMed ID: 19067405
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  • 11. Aortic arch anomalies associated with chromosome 22q11 deletion (CATCH 22).
    Momma K, Matsuoka R, Takao A.
    Pediatr Cardiol; 1999 Jan; 20(2):97-102. PubMed ID: 9986884
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  • 14. Absent or hypoplastic thymus on ultrasound: a marker for deletion 22q11.2 in fetal cardiac defects.
    Chaoui R, Kalache KD, Heling KS, Tennstedt C, Bommer C, Körner H.
    Ultrasound Obstet Gynecol; 2002 Dec; 20(6):546-52. PubMed ID: 12493042
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  • 15. Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome.
    Momma K, Kondo C, Matsuoka R, Takao A.
    Am J Cardiol; 1996 Sep 01; 78(5):591-4. PubMed ID: 8806353
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  • 19. Microdeletion 22q11 in complex cardiovascular malformations.
    Mehraein Y, Wippermann CF, Michel-Behnke I, Nhan Ngo TK, Hillig U, Giersberg M, Aulepp U, Barth H, Fritz B, Rehder H.
    Hum Genet; 1997 Apr 01; 99(4):433-42. PubMed ID: 9099830
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