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Journal Abstract Search

135 related items for PubMed ID: 11840485

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  • 5. Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome.
    Morrow B, Goldberg R, Carlson C, Das Gupta R, Sirotkin H, Collins J, Dunham I, O'Donnell H, Scambler P, Shprintzen R.
    Am J Hum Genet; 1995 Jun; 56(6):1391-403. PubMed ID: 7762562
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  • 8. 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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  • 9. 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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  • 11. Chromosome 22q11.2 deletion and phenotypic features in 30 patients with conotruncal heart defects.
    Derbent M, Yilmaz Z, Baltaci V, Saygili A, Varan B, Tokel K.
    Am J Med Genet A; 2003 Jan 15; 116A(2):129-35. PubMed ID: 12494430
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  • 14. Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery.
    Ziolkowska L, Kawalec W, Turska-Kmiec A, Krajewska-Walasek M, Brzezinska-Rajszys G, Daszkowska J, Maruszewski B, Burczynski P.
    Eur J Pediatr; 2008 Oct 15; 167(10):1135-40. PubMed ID: 18172682
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  • 20. 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 15; 30(10):807-12. PubMed ID: 7901419
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