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Journal Abstract Search

206 related items for PubMed ID: 7759065

  • 1. 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot.
    Amati F, Mari A, Digilio MC, Mingarelli R, Marino B, Giannotti A, Novelli G, Dallapiccola B.
    Hum Genet; 1995 May; 95(5):479-82. PubMed ID: 7759065
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  • 2. Frequency of 22q11.2 microdeletion in sporadic non-syndromic tetralogy of Fallot cases.
    Gioli-Pereira L, Pereira AC, Bergara D, Mesquita S, Lopes AA, Krieger JE.
    Int J Cardiol; 2008 Jun 06; 126(3):374-8. PubMed ID: 17604138
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  • 3. Molecular characterization of tetralogy of fallot within Digeorge critical region of the chromosome 22.
    Lu JH, Chung MY, Betau H, Chien HP, Lu JK.
    Pediatr Cardiol; 2001 Jun 06; 22(4):279-84. PubMed ID: 11455393
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  • 4. Frequency of a 22q11 deletion in patients with conotruncal cardiac malformations: a prospective study.
    Takahashi K, Kido S, Hoshino K, Ogawa K, Ohashi H, Fukushima Y.
    Eur J Pediatr; 1995 Nov 06; 154(11):878-81. PubMed ID: 8582397
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  • 7. A search for chromosome 22q11.2 deletions in a series of 176 consecutively catheterized patients with congenital heart disease: no evidence for deletions in non-syndromic patients.
    Borgmann S, Luhmer I, Arslan-Kirchner M, Kallfelz HC, Schmidtke J.
    Eur J Pediatr; 1999 Dec 06; 158(12):958-63. PubMed ID: 10592069
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  • 10. Classical Noonan syndrome is not associated with deletions of 22q11.
    Robin NH, Sellinger B, McDonald-McGinn D, Zackai EH, Emanuel BS, Driscoll DA.
    Am J Med Genet; 1995 Mar 13; 56(1):94-6. PubMed ID: 7747795
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  • 14. Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations.
    Ravnan JB, Chen E, Golabi M, Lebo RV.
    Am J Med Genet; 1996 Dec 18; 66(3):250-6. PubMed ID: 8985481
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  • 15. 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 18; 85(1):30-5. PubMed ID: 19067405
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  • 16. 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 18; 30(10):807-12. PubMed ID: 7901419
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