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Journal Abstract Search

178 related items for PubMed ID: 22523843

  • 21. VEGFA polymorphisms and cardiovascular anomalies in 22q11 microdeletion syndrome: a case-control and family-based study.
    Calderón JF, Puga AR, Guzmán ML, Astete CP, Arriaza M, Aracena M, Aravena T, Sanz P, Repetto GM.
    Biol Res; 2009; 42(4):461-8. PubMed ID: 20140301
    [Abstract] [Full Text] [Related]

  • 22. [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]

  • 23. [Diagnosis of 22q11 deletion and duplication in congenital heart disease by multiplex ligation dependent probe amplification].
    Yang YH, Hu YL, Zhu XY, Mo XM, Wang DJ, Yao JC, Sheng M, Zhu HY, Li J, Ru T, Wang ZQ.
    Zhongguo Dang Dai Er Ke Za Zhi; 2009 Nov; 11(11):892-6. PubMed ID: 20113655
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  • 25. Microdeletion 22q11 and oesophageal atresia.
    Digilio MC, Marino B, Bagolan P, Giannotti A, Dallapiccola B.
    J Med Genet; 1999 Feb; 36(2):137-9. PubMed ID: 10051013
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  • 26. 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 Feb; 42(3):215-8. PubMed ID: 11105620
    [Abstract] [Full Text] [Related]

  • 27. Association of consanguinity with congenital heart diseases in a teaching hospital in Western Iraq.
    Al-Ani ZR.
    Saudi Med J; 2010 Sep; 31(9):1021-7. PubMed ID: 20844815
    [Abstract] [Full Text] [Related]

  • 28. Clinical profile of patients with tetralogy of Fallot admitted for surgery at a cardiac surgical centre.
    Otaigbe BE, Kumar S.
    JNMA J Nepal Med Assoc; 2011 Sep; 51(182):62-6. PubMed ID: 22916514
    [Abstract] [Full Text] [Related]

  • 29. [Clinical detection of 22q11 microdeletion in the patients with congenital heart disease by multiplex ligation dependent probe amplification].
    Chen Y, Kan HJ, Mao J, Ding J, Meng QX, Li HB, Cheng HB, Liu MJ, Sun Y, Yan WH, Li H.
    Zhonghua Er Ke Za Zhi; 2011 Apr; 49(4):316-9. PubMed ID: 21624212
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  • 30. [22q11 microdeletion test in patients with congenital heart defects by quantitative fluorescent PCR].
    Chen Y, Mao J, Kwok KY, Kan HJ, Cheng HB, Li HB, Liu MJ, Sun Y, Yan WH, Li H, Choy KW.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Oct; 27(5):571-5. PubMed ID: 20931540
    [Abstract] [Full Text] [Related]

  • 31. [Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome].
    Muñoz S, Garay F, Flores I, Heusser F, Talesnik E, Aracena M, Mellado C, Méndez C, Arnaiz P, Repetto G.
    Rev Med Chil; 2001 May; 129(5):515-21. PubMed ID: 11464533
    [Abstract] [Full Text] [Related]

  • 32. 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 May; 45(3):217-20. PubMed ID: 14696799
    [Abstract] [Full Text] [Related]

  • 33. Chromosome 22q11 deletions in patients with selected outflow tract malformations.
    Frohn-Mulder IM, Wesby Swaay E, Bouwhuis C, Van Hemel JO, Gerritsma E, Niermeyer MF, Hess J.
    Genet Couns; 1999 May; 10(1):35-41. PubMed ID: 10191427
    [Abstract] [Full Text] [Related]

  • 34. Fragile X syndrome and 22q11.2 microdeletion in the same sibship.
    Missirian C, Moncla A, Voelckel MA, Ravix V, Philip N.
    Am J Med Genet; 2000 Dec 11; 95(4):358-60. PubMed ID: 11186890
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  • 36. Monozygotic twins with chromosome 22q11 microdeletion and discordant phenotypes in cardiovascular patterning.
    Lu JH, Chung MY, Hwang B, Chien HP.
    Pediatr Cardiol; 2001 Dec 11; 22(3):260-3. PubMed ID: 11343161
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  • 40. Catch 22--microdeletion 22q11 screening in patients with congenital heart defects.
    Von Beust G, Bartmus D, Bartels I.
    Genet Couns; 1998 Dec 11; 9(3):223-7. PubMed ID: 9777346
    [No Abstract] [Full Text] [Related]

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