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Journal Abstract Search

459 related items for PubMed ID: 15708709

  • 1. Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies.
    Beauchesne LM, Warnes CA, Connolly HM, Ammash NM, Grogan M, Jalal SM, Michels VV.
    J Am Coll Cardiol; 2005 Feb 15; 45(4):595-8. PubMed ID: 15708709
    [Abstract] [Full Text] [Related]

  • 2. Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion.
    Momma K, Kondo C, Matsuoka R.
    J Am Coll Cardiol; 1996 Jan 15; 27(1):198-202. PubMed ID: 8522695
    [Abstract] [Full Text] [Related]

  • 3. 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 15; 2(5):384-7. PubMed ID: 11392644
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. [22q11 deletion in conotruncal anomalies].
    Kádár K.
    Orv Hetil; 2005 Feb 20; 146(8):363-6. PubMed ID: 15803887
    [Abstract] [Full Text] [Related]

  • 6. [Microdeletion of 22q11 and conotruncal cardiopathies: contribution of prenatal diagnosis].
    Verspyck E, Joly G, Rossi A, David N, Blaysat G, Henocq A, Moirot H, Labadie G, Marpeau L.
    J Gynecol Obstet Biol Reprod (Paris); 1999 Oct 20; 28(6):534-7. PubMed ID: 10598346
    [Abstract] [Full Text] [Related]

  • 7. 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 20; 167(10):1135-40. PubMed ID: 18172682
    [Abstract] [Full Text] [Related]

  • 8. Congenital heart defects and chromosomal anomalies including 22q11 microdeletion (CATCH 22).
    Soares G, Alvares S, Rocha C, Teixeira MF, Mota MC, Reis MI, Feijó MJ, Lima MR, Pinto MR.
    Rev Port Cardiol; 2005 Mar 20; 24(3):349-71. PubMed ID: 15929620
    [Abstract] [Full Text] [Related]

  • 9. [Frequency of 22q11 deletions in children with isolated conotruncal defects].
    Shen L, Xu YJ, Zhao PJ, Sun K.
    Zhongguo Dang Dai Er Ke Za Zhi; 2009 Jan 20; 11(1):25-8. PubMed ID: 19149917
    [Abstract] [Full Text] [Related]

  • 10. 22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia.
    van Engelen K, Topf A, Keavney BD, Goodship JA, van der Velde ET, Baars MJ, Snijder S, Moorman AF, Postma AV, Mulder BJ.
    Heart; 2010 Apr 20; 96(8):621-4. PubMed ID: 20357389
    [Abstract] [Full Text] [Related]

  • 11. Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: a 6-year prospective study.
    Boudjemline Y, Fermont L, Le Bidois J, Lyonnet S, Sidi D, Bonnet D.
    J Pediatr; 2001 Apr 20; 138(4):520-4. PubMed ID: 11295715
    [Abstract] [Full Text] [Related]

  • 12. Cardiovascular anomalies in patients with chromosome 22q11.2 deletion: a Korean multicenter study.
    Park IS, Ko JK, Kim YH, Yoo HW, Seo EJ, Choi JY, Gil HY, Kim SJ.
    Int J Cardiol; 2007 Jan 08; 114(2):230-5. PubMed ID: 16824627
    [Abstract] [Full Text] [Related]

  • 13. Chromosome 22q11 deletions in patients with conotruncal heart defects.
    Khositseth A, Tocharoentanaphol C, Khowsathit P, Ruangdaraganon N.
    Pediatr Cardiol; 2005 Jan 08; 26(5):570-3. PubMed ID: 16132309
    [Abstract] [Full Text] [Related]

  • 14. Genetic background of congenital conotruncal heart defects--a study of 45 families.
    Kwiatkowska J, Wierzba J, Aleszewicz-Baranowska J, Ereciński J.
    Kardiol Pol; 2007 Jan 08; 65(1):32-7; discussion 38-9. PubMed ID: 17295158
    [Abstract] [Full Text] [Related]

  • 15. [Chromosome 22 (22q.11.2) deletion. Etiology of conotruncal heart abnormalities].
    Buendía Hernández A, Calderón-Colmenero J, Aizpuru E, Attie CL, Zabal C, Patiño E, Miranda I, Juanico A, Attie F.
    Arch Inst Cardiol Mex; 2000 Jan 08; 70(2):148-53. PubMed ID: 10932799
    [Abstract] [Full Text] [Related]

  • 16. 22q11.2 deletion mosaicism in patients with conotruncal heart defects.
    Jianrong L, Yinglong L, Xiaodong L, Cuntao Y, Bin C, Bo W.
    Birth Defects Res A Clin Mol Teratol; 2006 Apr 08; 76(4):262-5. PubMed ID: 16575883
    [Abstract] [Full Text] [Related]

  • 17. [Chromosome 22q11.2 microdeletion and phenotype analysis of patients with non-syndromic tetralogy of Fallot].
    Zhang ZW, Deng JY, Ying LY, Gao Z, Jin J, Qi JC, Tan Z.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec 08; 28(6):708-11. PubMed ID: 22161111
    [Abstract] [Full Text] [Related]

  • 18. 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 08; 32(2):492-8. PubMed ID: 9708481
    [Abstract] [Full Text] [Related]

  • 19. 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 08; 100(9):e97-100. PubMed ID: 21418101
    [Abstract] [Full Text] [Related]

  • 20. [Detection and related analysis to chromosome 22q11 microdeletion in patients with congenital heart diseases].
    Xu ZF, Yi L, Mo XM, Hu Y, Wang DJ, Zhu RF, Jiang YZ, Wu X, Wu Z, Shen L, Zhang Y, Zhong XL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun 08; 23(3):250-5. PubMed ID: 16767657
    [Abstract] [Full Text] [Related]

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