These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

343 related items for PubMed ID: 14696799

  • 1. Congenital cardiac defects with 22q11 deletion.
    Giray O, Ulgenalp A, Bora E, Sağin Saylam G, Unal N, Meşe T, Hüdaoğlu S, Erçal D.
    Turk J Pediatr; 2003; 45(3):217-20. PubMed ID: 14696799
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. 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; 65(1):32-7; discussion 38-9. PubMed ID: 17295158
    [Abstract] [Full Text] [Related]

  • 4. Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations.
    Alikaşifoğlu M, Malkoç N, Ceviz N, Ozme S, Uludoğan S, Tunçbilek E.
    Turk J Pediatr; 2000 Jan; 42(3):215-8. PubMed ID: 11105620
    [Abstract] [Full Text] [Related]

  • 5. [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; 28(6):534-7. PubMed ID: 10598346
    [Abstract] [Full Text] [Related]

  • 6. [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; 11(1):25-8. PubMed ID: 19149917
    [Abstract] [Full Text] [Related]

  • 7. Catch 22--microdeletion 22q11 screening in patients with congenital heart defects.
    Von Beust G, Bartmus D, Bartels I.
    Genet Couns; 1998 Jan; 9(3):223-7. PubMed ID: 9777346
    [No Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. [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 15; 23(3):250-5. PubMed ID: 16767657
    [Abstract] [Full Text] [Related]

  • 11. 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 15; 100(9):e97-100. PubMed ID: 21418101
    [Abstract] [Full Text] [Related]

  • 12. Incidences of micro-deletion/duplication 22q11.2 detected by multiplex ligation-dependent probe amplification in patients with congenital cardiac disease who are scheduled for cardiac surgery.
    Hu Y, Zhu X, Yang Y, Mo X, Sheng M, Yao J, Wang D.
    Cardiol Young; 2009 Apr 15; 19(2):179-84. PubMed ID: 19224675
    [Abstract] [Full Text] [Related]

  • 13. Chromosome 22q11 deletion syndrome: the first three cases reported in Thailand.
    Ruangdaraganon N, Tocharoentanaphol C, Khowsathit P, Sombuntham T, Pongpanich B.
    J Med Assoc Thai; 1999 Nov 15; 82 Suppl 1():S179-85. PubMed ID: 10730540
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 15. Microdeletion 22q11 and oesophageal atresia.
    Digilio MC, Marino B, Bagolan P, Giannotti A, Dallapiccola B.
    J Med Genet; 1999 Feb 15; 36(2):137-9. PubMed ID: 10051013
    [Abstract] [Full Text] [Related]

  • 16. Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland.
    Wozniak A, Wolnik-Brzozowska D, Wisniewska M, Glazar R, Materna-Kiryluk A, Moszura T, Badura-Stronka M, Skolozdrzy J, Krawczynski MR, Zeyland J, Bobkowski W, Slomski R, Latos-Bielenska A, Siwinska A.
    BMC Pediatr; 2010 Dec 06; 10():88. PubMed ID: 21134246
    [Abstract] [Full Text] [Related]

  • 17. 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 06; 76(4):262-5. PubMed ID: 16575883
    [Abstract] [Full Text] [Related]

  • 18. 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 06; 138(4):520-4. PubMed ID: 11295715
    [Abstract] [Full Text] [Related]

  • 19. [Search for 22q11 deletion and linkage study in familial cases of non-syndromic conotruncal defects].
    Debrus S.
    Arch Mal Coeur Vaiss; 1994 May 06; 87(5):657-61. PubMed ID: 7857190
    [Abstract] [Full Text] [Related]

  • 20. [Relationship between 22q11 microdeletion syndrome and congenital heart disease].
    Qin YF, Xie CH, Yang JB, Wu DW, Shao J, Zhao ZY.
    Zhonghua Xin Xue Guan Bing Za Zhi; 2011 Jul 06; 39(7):631-5. PubMed ID: 22088244
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 18.