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Journal Abstract Search

363 related items for PubMed ID: 34246755

  • 1. Whole-exome sequencing increases the diagnostic rate for prenatal fetal structural anomalies.
    Lei L, Zhou L, Xiong JJ.
    Eur J Med Genet; 2021 Sep; 64(9):104288. PubMed ID: 34246755
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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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  • 7. Whole-exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonography.
    Lei TY, Fu F, Li R, Yu QX, Du K, Zhang WW, Deng Q, Li LS, Wang D, Yang X, Zhen L, Li DZ, Liao C.
    Prenat Diagn; 2020 Sep 23; 40(10):1290-1299. PubMed ID: 32436246
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  • 8. Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES).
    Leung GKC, Mak CCY, Fung JLF, Wong WHS, Tsang MHY, Yu MHC, Pei SLC, Yeung KS, Mok GTK, Lee CP, Hui APW, Tang MHY, Chan KYK, Liu APY, Yang W, Sham PC, Kan ASY, Chung BHY.
    BMC Med Genomics; 2018 Oct 25; 11(1):93. PubMed ID: 30359267
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  • 17. Prenatal diagnosis of skeletal dysplasias using whole exome sequencing in China.
    Tang J, Zhou C, Shi H, Mo Y, Tan W, Sun T, Zhu J, Li Q, Li H, Li Y, Wang S, Hong Y, Li N, Zeng Q, Tan J, Ma W, Luo L.
    Clin Chim Acta; 2020 Aug 25; 507():187-193. PubMed ID: 32360156
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  • 18. Whole Exome Sequencing: Applications in Prenatal Genetics.
    Jelin AC, Vora N.
    Obstet Gynecol Clin North Am; 2018 Mar 25; 45(1):69-81. PubMed ID: 29428287
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  • 19. [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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  • 20. The Added Value of Whole-Exome Sequencing for Anomalous Fetuses With Detailed Prenatal Ultrasound and Postnatal Phenotype.
    He M, Du L, Xie H, Zhang L, Gu Y, Lei T, Zheng J, Chen D.
    Front Genet; 2021 Jul 25; 12():627204. PubMed ID: 34367232
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