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530 related items for PubMed ID: 31060568

  • 1. Genetic anomalies in fetuses with tetralogy of Fallot by using high-definition chromosomal microarray analysis.
    Peng R, Zheng J, Xie HN, He M, Lin MF.
    Cardiovasc Ultrasound; 2019 May 06; 17(1):8. PubMed ID: 31060568
    [Abstract] [Full Text] [Related]

  • 2. Fetal cardiac axis in tetralogy of Fallot: associations with prenatal findings, genetic anomalies and postnatal outcome.
    Zhao Y, Edington S, Fleenor J, Sinkovskaya E, Porche L, Abuhamad A.
    Ultrasound Obstet Gynecol; 2017 Jul 06; 50(1):58-62. PubMed ID: 27302537
    [Abstract] [Full Text] [Related]

  • 3. Fetal right aortic arch: associated anomalies, genetic anomalies with chromosomal microarray analysis, and postnatal outcome.
    Peng R, Xie HN, Zheng J, Zhou Y, Lin MF.
    Prenat Diagn; 2017 Apr 06; 37(4):329-335. PubMed ID: 28165153
    [Abstract] [Full Text] [Related]

  • 4. Assessment of cardiac angle in fetuses with congenital heart disease at risk of 22q11.2 deletion.
    Vigneswaran TV, Kametas NA, Zinevich Y, Bataeva R, Allan LD, Zidere V.
    Ultrasound Obstet Gynecol; 2015 Dec 06; 46(6):695-9. PubMed ID: 25720805
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  • 8. Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis.
    Mademont-Soler I, Morales C, Soler A, Martínez-Crespo JM, Shen Y, Margarit E, Clusellas N, Obón M, Wu BL, Sánchez A.
    Ultrasound Obstet Gynecol; 2013 Apr 06; 41(4):375-82. PubMed ID: 23233332
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  • 10. Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center retrospective study.
    Zhuang J, Zhang N, Chen Y, Jiang Y, Chen X, Chen W, Chen C.
    Sci Rep; 2024 Jan 27; 14(1):2271. PubMed ID: 38280885
    [Abstract] [Full Text] [Related]

  • 11. Association of prenatal renal ultrasound abnormalities with pathogenic copy number variants in a large Chinese cohort.
    Su J, Qin Z, Fu H, Luo J, Huang Y, Huang P, Zhang S, Liu T, Lu W, Li W, Jiang T, Wei S, Yang S, Shen Y.
    Ultrasound Obstet Gynecol; 2022 Feb 27; 59(2):226-233. PubMed ID: 34090309
    [Abstract] [Full Text] [Related]

  • 12. Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis.
    Xie X, Huang B, Su L, Cai M, Chen Y, Wu X, Xu L.
    BMC Med Genomics; 2023 Nov 20; 16(1):298. PubMed ID: 37986075
    [Abstract] [Full Text] [Related]

  • 13. Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing.
    Zhu X, Li J, Ru T, Wang Y, Xu Y, Yang Y, Wu X, Cram DS, Hu Y.
    Prenat Diagn; 2016 Apr 20; 36(4):321-7. PubMed ID: 26833920
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  • 14. [Prenatal diagnosis of heart defects and associated chromosomal aberrations].
    Chaoui R, Körner H, Bommer C, Göldner B, Bierlich A, Bollmann R.
    Ultraschall Med; 1999 Oct 20; 20(5):177-84. PubMed ID: 10595385
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  • 15. Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype.
    Wu X, Li Y, Su L, Xie X, Cai M, Lin N, Huang H, Lin Y, Xu L.
    Mol Diagn Ther; 2020 Oct 20; 24(5):611-619. PubMed ID: 32651932
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  • 16. Tetralogy of Fallot in the fetus in the current era.
    Poon LC, Huggon IC, Zidere V, Allan LD.
    Ultrasound Obstet Gynecol; 2007 Jun 20; 29(6):625-7. PubMed ID: 17405110
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  • 17. Prenatal diagnosis of submicroscopic chromosomal aberrations in fetuses with ventricular septal defects by chromosomal microarray-based analysis.
    Du L, Xie HN, Huang LH, Xie YJ, Wu LH.
    Prenat Diagn; 2016 Dec 20; 36(13):1178-1184. PubMed ID: 27794163
    [Abstract] [Full Text] [Related]

  • 18. Chromosomal abnormalities among children born with conotruncal cardiac defects.
    Lammer EJ, Chak JS, Iovannisci DM, Schultz K, Osoegawa K, Yang W, Carmichael SL, Shaw GM.
    Birth Defects Res A Clin Mol Teratol; 2009 Jan 20; 85(1):30-5. PubMed ID: 19067405
    [Abstract] [Full Text] [Related]

  • 19. Prenatal diagnosis in fetal right aortic arch using chromosomal microarray analysis and whole exome sequencing: a Chinese single-center retrospective study.
    Zhang L, Huang R, Zhou H, Lin X, Guo F, Jing X, Zhang Y, Li F, Li F, Yu Q, Wang D, Chen G, Fu F, Pan M, Han J, Li D, Li R.
    Mol Cytogenet; 2024 Sep 27; 17(1):22. PubMed ID: 39334424
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  • 20. Prenatal diagnosis of chromosomal aberrations in fetuses with conotruncal heart defects by genome-wide high-resolution SNP array.
    Lin M, Zheng J, Peng R, Du L, Zheng Q, Lei T, Xie H.
    J Matern Fetal Neonatal Med; 2020 Apr 27; 33(7):1211-1217. PubMed ID: 30149741
    [Abstract] [Full Text] [Related]

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