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236 related items for PubMed ID: 25215544

  • 1. Detection of chromosomal abnormalities and the 22q11 microdeletion in fetuses with congenital heart defects.
    Lv W, Wang S.
    Mol Med Rep; 2014 Nov; 10(5):2465-70. PubMed ID: 25215544
    [Abstract] [Full Text] [Related]

  • 2. [Prenatal genetic study of fetuses with congenital heart diseases].
    Xu ZF, Cao L, Ji XQ, Yang C, Zhang JJ, Xu QJ, Zha W, Yang YQ, Lin YS, Chen CH, Liu A, Li L, Lin Y, Yi L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):128-33. PubMed ID: 19350500
    [Abstract] [Full Text] [Related]

  • 3. 22q11 deletions in fetuses with malformations of the outflow tracts or interruption of the aortic arch: impact of additional ultrasound signs.
    Volpe P, Marasini M, Caruso G, Marzullo A, Buonadonna AL, Arciprete P, Di Paolo S, Volpe G, Gentile M.
    Prenat Diagn; 2003 Sep; 23(9):752-7. PubMed ID: 12975788
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  • 4. Investigating 22q11.2 deletion and other chromosomal aberrations in fetuses with heart defects detected by prenatal echocardiography.
    Bellucco FT, Belangero SI, Farah LM, Machado MV, Cruz AP, Lopes LM, Lopes MA, Zugaib M, Cernach MC, Melaragno MI.
    Pediatr Cardiol; 2010 Nov; 31(8):1146-50. PubMed ID: 20848279
    [Abstract] [Full Text] [Related]

  • 5. 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; 24(3):349-71. PubMed ID: 15929620
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  • 7. [Study on the relationship between 22q11 microdeletion and congenital heart disease].
    Du YR, Yang HJ, Tan Z, Huang Y, Li SL, Tian JW, Zhang GY, Li P, Fu SB.
    Yi Chuan; 2005 Nov; 27(6):873-6. PubMed ID: 16378931
    [Abstract] [Full Text] [Related]

  • 8. MLPA: a prenatal diagnostic tool for the study of congenital heart defects?
    Mademont-Soler I, Morales C, Soler A, Clusellas N, Margarit E, Martínez-Barrios E, Martínez JM, Sánchez A.
    Gene; 2012 May 25; 500(1):151-4. PubMed ID: 22446045
    [Abstract] [Full Text] [Related]

  • 9. Prenatal diagnosis of aneuploidy and deletion 22q11.2 in fetuses with ultrasound detection of cardiac defects.
    Moore JW, Binder GA, Berry R.
    Am J Obstet Gynecol; 2004 Dec 25; 191(6):2068-73. PubMed ID: 15592293
    [Abstract] [Full Text] [Related]

  • 10. The thymic-thoracic ratio in fetal heart defects: a simple way to identify fetuses at high risk for microdeletion 22q11.
    Chaoui R, Heling KS, Lopez AS, Thiel G, Karl K.
    Ultrasound Obstet Gynecol; 2011 Apr 25; 37(4):397-403. PubMed ID: 21308838
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
    Kuo YL, Chen CP, Wang LK, Ko TM, Chang TY, Chern SR, Wu PS, Chen YT, Chang SY.
    Taiwan J Obstet Gynecol; 2014 Jun 25; 53(2):248-51. PubMed ID: 25017279
    [Abstract] [Full Text] [Related]

  • 12. [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 25; 39(7):631-5. PubMed ID: 22088244
    [Abstract] [Full Text] [Related]

  • 13. Extracardiac lesions and chromosomal abnormalities associated with major fetal heart defects: comparison of intrauterine, postnatal and postmortem diagnoses.
    Song MS, Hu A, Dyamenahalli U, Chitayat D, Winsor EJ, Ryan G, Smallhorn J, Barrett J, Yoo SJ, Hornberger LK.
    Ultrasound Obstet Gynecol; 2009 May 25; 33(5):552-9. PubMed ID: 19350566
    [Abstract] [Full Text] [Related]

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  • 16. 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 25; 45(3):217-20. PubMed ID: 14696799
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  • 18. Use of amniocytes for prenatal diagnosis of 22q11.2 microdeletion syndrome: a feasibility study.
    Liu T, Liu Q, Wang YX, Yang D, Xin Y, Fang Z, Ding SF, Yang JF.
    Chin Med J (Engl); 2010 Feb 20; 123(4):438-42. PubMed ID: 20193483
    [Abstract] [Full Text] [Related]

  • 19. Prenatal and postnatal diagnosis of 22q11.2 deletion syndrome.
    Bretelle F, Beyer L, Pellissier MC, Missirian C, Sigaudy S, Gamerre M, D'Ercole C, Philip N.
    Eur J Med Genet; 2010 Feb 20; 53(6):367-70. PubMed ID: 20659598
    [Abstract] [Full Text] [Related]

  • 20. [Prenatal diagnosis of 22q11.2 microdeletion by multiplex ligation-dependent probe amplification].
    Luo CY, Ma DY, Zhang JJ, Hu P, Cao L, Ji XQ, Zhou J, Liu A, Wu Y, Cheng J, Lin Y, Xu ZF.
    Zhonghua Fu Chan Ke Za Zhi; 2013 Nov 20; 48(11):824-7. PubMed ID: 24444558
    [Abstract] [Full Text] [Related]

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