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Journal Abstract Search

203 related items for PubMed ID: 36609702

  • 1. Chromosomal abnormalities in fetuses with congenital heart disease: a meta-analysis.
    Wang H, Lin X, Lyu G, He S, Dong B, Yang Y.
    Arch Gynecol Obstet; 2023 Sep; 308(3):797-811. PubMed ID: 36609702
    [Abstract] [Full Text] [Related]

  • 2. Comprehensive evaluation of genetic variants using chromosomal microarray analysis and exome sequencing in fetuses with congenital heart defect.
    Qiao F, Wang Y, Zhang C, Zhou R, Wu Y, Wang C, Meng L, Mao P, Cheng Q, Luo C, Hu P, Xu Z.
    Ultrasound Obstet Gynecol; 2021 Sep; 58(3):377-387. PubMed ID: 33142350
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease.
    Yan Y, Wu Q, Zhang L, Wang X, Dan S, Deng D, Sun L, Yao L, Ma Y, Wang L.
    Ultrasound Obstet Gynecol; 2014 Apr; 43(4):404-12. PubMed ID: 24323407
    [Abstract] [Full Text] [Related]

  • 5. Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysis.
    Jansen FA, Blumenfeld YJ, Fisher A, Cobben JM, Odibo AO, Borrell A, Haak MC.
    Ultrasound Obstet Gynecol; 2015 Jan; 45(1):27-35. PubMed ID: 25319878
    [Abstract] [Full Text] [Related]

  • 6. Prenatal chromosomal microarray analysis in a large Chinese cohort of fetuses with congenital heart defects: a single center study.
    Lu Q, Luo L, Zeng B, Luo H, Wang X, Qiu L, Yang Y, Feng C, Zhou J, Hu Y, Huang T, Ma P, Huang T, Xie K, Yuan H, Huang S, Yang B, Zou Y, Liu Y.
    Orphanet J Rare Dis; 2024 Aug 22; 19(1):307. PubMed ID: 39175064
    [Abstract] [Full Text] [Related]

  • 7. [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 22; 26(2):128-33. PubMed ID: 19350500
    [Abstract] [Full Text] [Related]

  • 8.
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  • 9. [Clinical value of genome-wide high resolution chromosomal microarray analysis in etiological study of fetuses with congenital heart defects].
    Wu X, Fu F, Li R, Pan M, Han J, Zhen L, Yang X, Zhang Y, Li F, Liao C.
    Zhonghua Fu Chan Ke Za Zhi; 2014 Dec 22; 49(12):893-8. PubMed ID: 25608988
    [Abstract] [Full Text] [Related]

  • 10. Genetic Testing and Pregnancy Outcome Analysis of 362 Fetuses with Congenital Heart Disease Identified by Prenatal Ultrasound.
    Luo S, Meng D, Li Q, Hu X, Chen Y, He C, Xie B, She S, Li Y, Fu C.
    Arq Bras Cardiol; 2018 Oct 22; 111(4):571-577. PubMed ID: 30133550
    [Abstract] [Full Text] [Related]

  • 11.
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  • 12. Prevalence of chromosomal abnormalities and 22q11.2 deletion in conotruncal and non-conotruncal antenatally diagnosed congenital heart diseases in a Chinese population.
    Kong CW, Cheng YKY, To WWK, Leung TY.
    Hong Kong Med J; 2019 Feb 22; 25(1):6-12. PubMed ID: 30655461
    [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 22; 36(4):321-7. PubMed ID: 26833920
    [Abstract] [Full Text] [Related]

  • 14. Chromosomal microarray analysis for the detection of chromosome abnormalities in fetuses with echogenic intracardiac focus in women without high-risk factors.
    He M, Zhang Z, Hu T, Liu S.
    Medicine (Baltimore); 2020 Jan 22; 99(5):e19014. PubMed ID: 32000445
    [Abstract] [Full Text] [Related]

  • 15. Chromosomal microarray analysis in the investigation of prenatally diagnosed congenital heart disease.
    Mustafa HJ, Jacobs KM, Tessier KM, Narasimhan SL, Tofte AN, McCarter AR, Cross SN.
    Am J Obstet Gynecol MFM; 2020 Feb 22; 2(1):100078. PubMed ID: 33345990
    [Abstract] [Full Text] [Related]

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

  • 17. Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome.
    Cai M, Huang H, Su L, Lin N, Wu X, Xie X, An G, Li Y, Lin Y, Xu L.
    Medicine (Baltimore); 2018 Dec 22; 97(50):e13617. PubMed ID: 30558042
    [Abstract] [Full Text] [Related]

  • 18. 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 22; 33(7):1211-1217. PubMed ID: 30149741
    [Abstract] [Full Text] [Related]

  • 19. [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 22; 20(5):177-84. PubMed ID: 10595385
    [Abstract] [Full Text] [Related]

  • 20. Chromosomal abnormalities and copy number variations in fetal left-sided congenital heart defects.
    Jansen FA, Hoffer MJ, van Velzen CL, Plati SK, Rijlaarsdam ME, Clur SA, Blom NA, Pajkrt E, Bhola SL, Knegt AC, de Boer MA, Haak MC.
    Prenat Diagn; 2016 Feb 22; 36(2):177-85. PubMed ID: 26716421
    [Abstract] [Full Text] [Related]

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