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Journal Abstract Search

218 related items for PubMed ID: 36923788

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  • 2. Prenatal diagnosis of genetic aberrations in fetuses with short femur detected by ultrasound: A prospective cohort study.
    Li Q, Zhang Z, Wang J, Zhang H, Zhu H, Lai Y, Liu S, Wang H, Hu T.
    Prenat Diagn; 2021 Aug; 41(9):1153-1163. PubMed ID: 34185917
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  • 4. Diagnostic Yield of Exome Sequencing in Fetuses with Sonographic Features of Skeletal Dysplasias but Normal Karyotype or Chromosomal Microarray Analysis: A Systematic Review.
    Tse KY, Surya IU, Irwinda R, Leung KY, Ting YH, Cao Y, Choy KW.
    Genes (Basel); 2023 May 30; 14(6):. PubMed ID: 37372383
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  • 5. Utility of trio-based prenatal exome sequencing incorporating splice-site and mitochondrial genome assessment in pregnancies with fetal ultrasound anomalies: prospective cohort study.
    Zhu X, Gao Z, Wang Y, Huang W, Li Q, Jiao Z, Liu N, Kong X.
    Ultrasound Obstet Gynecol; 2022 Dec 30; 60(6):780-792. PubMed ID: 35726512
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  • 9. Value of Exome Sequencing in Diagnosis and Management of Recurrent Non-immune Hydrops Fetalis: A Retrospective Analysis.
    Zhou X, Zhou J, Wei X, Yao R, Yang Y, Deng L, Zou G, Wang X, Yang Y, Duan T, Wang J, Sun L.
    Front Genet; 2021 Dec 30; 12():616392. PubMed ID: 33897756
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  • 10. Rapid prenatal diagnosis of skeletal dysplasia using medical trio exome sequencing: Benefit for prenatal counseling and pregnancy management.
    Han J, Yang YD, He Y, Liu WJ, Zhen L, Pan M, Yang X, Zhang VW, Liao C, Li DZ.
    Prenat Diagn; 2020 Apr 30; 40(5):577-584. PubMed ID: 31994750
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  • 11. Clinical application of medical exome sequencing for prenatal diagnosis of fetal structural anomalies.
    Chen M, Chen J, Wang C, Chen F, Xie Y, Li Y, Li N, Wang J, Zhang VW, Chen D.
    Eur J Obstet Gynecol Reprod Biol; 2020 Aug 30; 251():119-124. PubMed ID: 32502767
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  • 12. Whole exome sequencing as a diagnostic adjunct to clinical testing in fetuses with structural abnormalities.
    Fu F, Li R, Li Y, Nie ZQ, Lei T, Wang D, Yang X, Han J, Pan M, Zhen L, Ou Y, Li J, Li FT, Jing X, Li D, Liao C.
    Ultrasound Obstet Gynecol; 2018 Apr 30; 51(4):493-502. PubMed ID: 28976722
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  • 15. Should prenatal chromosomal microarray analysis be offered for isolated fetal growth restriction? A French multicenter study.
    Monier I, Receveur A, Houfflin-Debarge V, Goua V, Castaigne V, Jouannic JM, Mousty E, Saliou AH, Bouchghoul H, Rousseau T, Valat AS, Groussolles M, Fuchs F, Benoist G, Degre S, Massardier J, Tsatsaris V, Kleinfinger P, Zeitlin J, Benachi A, French Federation of Fetal Medicine Centers.
    Am J Obstet Gynecol; 2021 Dec 30; 225(6):676.e1-676.e15. PubMed ID: 34058167
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  • 16. Prenatal trio-based whole exome sequencing in fetuses with abnormalities of the skeletal system.
    Yang Y, Wang M, Wang H.
    Mol Genet Genomics; 2022 Jul 30; 297(4):1017-1026. PubMed ID: 35583673
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  • 17. Molecular diagnosis for 55 fetuses with skeletal dysplasias by whole-exome sequencing: A retrospective cohort study.
    Zhang L, Pan L, Teng Y, Liang D, Li Z, Wu L.
    Clin Genet; 2021 Aug 30; 100(2):219-226. PubMed ID: 33942288
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