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Journal Abstract Search

265 related items for PubMed ID: 37880672

  • 1. Prenatal whole-exome sequencing for fetal structural anomalies: a retrospective analysis of 145 Chinese cases.
    Qin Y, Yao Y, Liu N, Wang B, Liu L, Li H, Gao T, Xu R, Wang X, Zhang F, Song J.
    BMC Med Genomics; 2023 Oct 25; 16(1):262. PubMed ID: 37880672
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  • 2. Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
    Lord J, McMullan DJ, Eberhardt RY, Rinck G, Hamilton SJ, Quinlan-Jones E, Prigmore E, Keelagher R, Best SK, Carey GK, Mellis R, Robart S, Berry IR, Chandler KE, Cilliers D, Cresswell L, Edwards SL, Gardiner C, Henderson A, Holden ST, Homfray T, Lester T, Lewis RA, Newbury-Ecob R, Prescott K, Quarrell OW, Ramsden SC, Roberts E, Tapon D, Tooley MJ, Vasudevan PC, Weber AP, Wellesley DG, Westwood P, White H, Parker M, Williams D, Jenkins L, Scott RH, Kilby MD, Chitty LS, Hurles ME, Maher ER, Prenatal Assessment of Genomes and Exomes Consortium.
    Lancet; 2019 Feb 23; 393(10173):747-757. PubMed ID: 30712880
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  • 3. Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
    Petrovski S, Aggarwal V, Giordano JL, Stosic M, Wou K, Bier L, Spiegel E, Brennan K, Stong N, Jobanputra V, Ren Z, Zhu X, Mebane C, Nahum O, Wang Q, Kamalakaran S, Malone C, Anyane-Yeboa K, Miller R, Levy B, Goldstein DB, Wapner RJ.
    Lancet; 2019 Feb 23; 393(10173):758-767. PubMed ID: 30712878
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  • 5. Implementation of exome sequencing in fetal diagnostics-Data and experiences from a tertiary center in Denmark.
    Becher N, Andreasen L, Sandager P, Lou S, Petersen OB, Christensen R, Vogel I.
    Acta Obstet Gynecol Scand; 2020 Jun 23; 99(6):783-790. PubMed ID: 32304219
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  • 7. [Study of genetic etiology in fetuses with severely short limbs in the first and second trimester using whole exome sequencing].
    Zhang XY, You YQ, Zhou HH, Wang SJ, Xie XX, Zhang ML, Wang LX, Lu YP.
    Zhonghua Fu Chan Ke Za Zhi; 2019 Apr 25; 54(4):221-225. PubMed ID: 31006186
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  • 9. Whole-exome sequencing in deceased fetuses with ultrasound anomalies: a retrospective analysis.
    Huang W, Zhu X, Sun G, Gao Z, Kong X.
    BMC Med Genomics; 2023 Feb 16; 16(1):25. PubMed ID: 36797717
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  • 10. Molecular diagnostic yield of exome sequencing in a Chinese cohort of 512 fetuses with anomalies.
    Jin P, Hong J, Xu Y, Qian Y, Han S, Dong M.
    BMC Pregnancy Childbirth; 2024 Sep 09; 24(1):591. PubMed ID: 39251974
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  • 15. [Analysis of families with fetal congenital abnormalities but negative prenatal diagnosis by whole exome sequencing].
    Fu F, Li LS, Du K, Li R, Yu QX, Wang D, Lei TY, Deng Q, Nie ZQ, Zhang WW, Yang X, Han J, Zhen L, Pan M, Zhang LN, Li FC, Zhang YL, Jing XY, Li DZ, Liao C.
    Zhonghua Fu Chan Ke Za Zhi; 2021 Jul 25; 56(7):458-466. PubMed ID: 34304437
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  • 16. Whole exome sequencing in fetuses with isolated increased nuchal translucency: a systematic review and meta-analysis.
    Di Girolamo R, Rizzo G, Khalil A, Alameddine S, Lisi G, Liberati M, Novelli A, D'Antonio F.
    J Matern Fetal Neonatal Med; 2023 Dec 25; 36(1):2193285. PubMed ID: 37019452
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  • 17. Whole-exome sequencing for prenatal diagnosis of fetuses with congenital anomalies of the kidney and urinary tract.
    Lei TY, Fu F, Li R, Wang D, Wang RY, Jing XY, Deng Q, Li ZZ, Liu ZQ, Yang X, Li DZ, Liao C.
    Nephrol Dial Transplant; 2017 Oct 01; 32(10):1665-1675. PubMed ID: 28387813
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  • 19. Rapid whole exome sequencing in pregnancies to identify the underlying genetic cause in fetuses with congenital anomalies detected by ultrasound imaging.
    Deden C, Neveling K, Zafeiropopoulou D, Gilissen C, Pfundt R, Rinne T, de Leeuw N, Faas B, Gardeitchik T, Sallevelt SCEH, Paulussen A, Stevens SJC, Sikkel E, Elting MW, van Maarle MC, Diderich KEM, Corsten-Janssen N, Lichtenbelt KD, Lachmeijer G, Vissers LELM, Yntema HG, Nelen M, Feenstra I, van Zelst-Stams WAG.
    Prenat Diagn; 2020 Jul 01; 40(8):972-983. PubMed ID: 32333414
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