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237 related items for PubMed ID: 34472185

  • 1. Congenital heart defects and copy number variants associated with neurodevelopmental impairment.
    Findley TO, Crain AK, Mahajan S, Deniwar A, Davis J, Solis Zavala AS, Corno AF, Rodriguez-Buritica D.
    Am J Med Genet A; 2022 Jan; 188(1):13-23. PubMed ID: 34472185
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  • 3. [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; 49(12):893-8. PubMed ID: 25608988
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  • 4. Detection of copy number variants using chromosomal microarray analysis for the prenatal diagnosis of congenital heart defects with normal karyotype.
    Song T, Wan S, Li Y, Xu Y, Dang Y, Zheng Y, Li C, Zheng J, Chen B, Zhang J.
    J Clin Lab Anal; 2019 Jan; 33(1):e22630. PubMed ID: 30047171
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  • 6. 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; 36(4):321-7. PubMed ID: 26833920
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  • 8. Chromosome microarray testing for patients with congenital heart defects reveals novel disease causing loci and high diagnostic yield.
    Geng J, Picker J, Zheng Z, Zhang X, Wang J, Hisama F, Brown DW, Mullen MP, Harris D, Stoler J, Seman A, Miller DT, Fu Q, Roberts AE, Shen Y.
    BMC Genomics; 2014 Dec 17; 15(1):1127. PubMed ID: 25516202
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  • 9. Chromosomal microarray detects genetic risks of neurodevelopmental disorders in newborns with congenital heart disease.
    Gill K, Sasaki J, Jayakar P, Sosa L, Welch E.
    Cardiol Young; 2021 Aug 17; 31(8):1275-1282. PubMed ID: 33536103
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  • 11. Chromosomal microarray testing yield in 829 cases of microcephaly: a clinical characteristics-based analysis for prenatal and postnatal cases.
    Sukenik-Halevy R, Mevorach N, Basel-Salmon L, Matar RT, Kahana S, Klein K, Agmon-Fishman I, Levy M, Maya I.
    Arch Gynecol Obstet; 2024 Sep 17; 310(3):1547-1554. PubMed ID: 38494511
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  • 12. Chromosomal microarray analysis in fetuses with an isolated congenital heart defect: A retrospective, nationwide, multicenter study in France.
    Hureaux M, Guterman S, Hervé B, Till M, Jaillard S, Redon S, Valduga M, Coutton C, Missirian C, Prieur F, Simon-Bouy B, Beneteau C, Kuentz P, Rooryck C, Gruchy N, Marle N, Plutino M, Tosca L, Dupont C, Puechberty J, Schluth-Bolard C, Salomon L, Sanlaville D, Malan V, Vialard F.
    Prenat Diagn; 2019 May 17; 39(6):464-470. PubMed ID: 30896039
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  • 13. 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 17; 43(4):404-12. PubMed ID: 24323407
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  • 15. Copy number variant analysis for syndromic congenital heart disease in the Chinese population.
    Li P, Chen W, Li M, Zhao Z, Feng Z, Gao H, Suo M, Xu Z, Tian G, Wu F, Wei S, Huang G.
    Hum Genomics; 2022 Oct 31; 16(1):51. PubMed ID: 36316717
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  • 16. Genetic testing practices in infants with congenital heart disease.
    Connor JA, Hinton RB, Miller EM, Sund KL, Ruschman JG, Ware SM.
    Congenit Heart Dis; 2014 Oct 31; 9(2):158-67. PubMed ID: 23782710
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  • 17. Clinical aspects of prenatally detected congenital heart malformations and the yield of chromosomal microarray analysis.
    Sukenik-Halevy R, Sukenik S, Koifman A, Alpert Y, Hershkovitz R, Levi A, Biron-Shental T.
    Prenat Diagn; 2016 Dec 31; 36(13):1185-1191. PubMed ID: 27794172
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  • 18. 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 31; 97(50):e13617. PubMed ID: 30558042
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  • 19. Genetic aetiology distribution of 398 foetuses with congenital heart disease in the prenatal setting.
    Yi T, Hao X, Sun H, Zhang Y, Han J, Gu X, Sun L, Liu X, Zhao Y, Guo Y, Zhou X, He Y.
    ESC Heart Fail; 2023 Apr 31; 10(2):917-930. PubMed ID: 36478645
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  • 20. The yield of SNP microarray analysis for fetal ultrasound cardiac abnormalities.
    Ye F, Xu X, Wang Y, Chen L, Shan Q, Wang Q, Jin F.
    BMC Pregnancy Childbirth; 2024 Apr 05; 24(1):244. PubMed ID: 38580914
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