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Journal Abstract Search

215 related items for PubMed ID: 37980516

  • 1. Analysis of genetic testing in fetuses with congenital heart disease of single atria and/or single ventricle in a Chinese prenatal cohort.
    Li M, Ye B, Chen Y, Gao L, Wu Y, Cheng W.
    BMC Pediatr; 2023 Nov 18; 23(1):577. PubMed ID: 37980516
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Yield rate of chromosomal microarray analysis in fetuses with congenital heart defects.
    Turan S, Asoglu MR, Gabbay-Benziv R, Doyle L, Harman C, Turan OM.
    Eur J Obstet Gynecol Reprod Biol; 2018 Feb 22; 221():172-176. PubMed ID: 29306563
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  • 4. 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 22; 58(3):377-387. PubMed ID: 33142350
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  • 6. Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China.
    Zhou Y, Lu X, Zhang Y, Ge Y, Xu Y, Wu L, Jiang Y.
    Cytogenet Genome Res; 2022 Sep 22; 162(7):354-364. PubMed ID: 36907182
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  • 7. 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 22; 36(1):2193285. PubMed ID: 37019452
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  • 10. Prenatal diagnosis for fetuses with isolated and non-isolated congenital heart defects using chromosomal microarray and exome sequencing.
    Xing Y, Zhang Y, Chen J, Wu F, Yuan M, Zou G, Yang Y, Zhou F, Zhou J, Sun L.
    Prenat Diagn; 2022 Jun 22; 42(7):873-880. PubMed ID: 35584285
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  • 11. 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 22; 51(4):493-502. PubMed ID: 28976722
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  • 12. Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes.
    Al-Hamed MH, Kurdi W, Khan R, Tulbah M, AlNemer M, AlSahan N, AlMugbel M, Rafiullah R, Assoum M, Monies D, Shah Z, Rahbeeni Z, Derar N, Hakami F, Almutairi G, AlOtaibi A, Ali W, AlShammasi A, AlMubarak W, AlDawoud S, AlAmri S, Saeed B, Bukhari H, Ali M, Akili R, Alquayt L, Hagos S, Elbardisy H, Akilan A, Almuhana N, AlKhalifah A, Abouelhoda M, Ramzan K, Sayer JA, Imtiaz F.
    Hum Genet; 2022 Jan 22; 141(1):101-126. PubMed ID: 34853893
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  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. Congenital hypotonia: systematic approach for prenatal detection.
    Weissbach T, Hausman-Kedem M, Yanay Z, Meyer R, Bar-Yosef O, Leibovitch L, Berkenstadt M, Chorin O, Shani H, Massarwa A, Achiron R, Weisz B, Sharon R, Mazaki-Tovi S, Kassif E.
    Ultrasound Obstet Gynecol; 2023 Jul 23; 62(1):94-105. PubMed ID: 36779229
    [Abstract] [Full Text] [Related]

  • 16. [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
    [Abstract] [Full Text] [Related]

  • 17. [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 25; 49(12):893-8. PubMed ID: 25608988
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  • 18. Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis.
    Mademont-Soler I, Morales C, Soler A, Martínez-Crespo JM, Shen Y, Margarit E, Clusellas N, Obón M, Wu BL, Sánchez A.
    Ultrasound Obstet Gynecol; 2013 Apr 25; 41(4):375-82. PubMed ID: 23233332
    [Abstract] [Full Text] [Related]

  • 19. Contribution of single-gene defects to congenital cardiac left-sided lesions in the prenatal setting.
    Sun H, Yi T, Hao X, Yan H, Wang J, Li Q, Gu X, Zhou X, Wang S, Wang X, Wan P, Han L, Chen J, Zhu H, Zhang H, He Y.
    Ultrasound Obstet Gynecol; 2020 Aug 25; 56(2):225-232. PubMed ID: 31633846
    [Abstract] [Full Text] [Related]

  • 20. Incremental yield of whole-genome sequencing over chromosomal microarray analysis and exome sequencing for congenital anomalies in prenatal period and infancy: systematic review and meta-analysis.
    Shreeve N, Sproule C, Choy KW, Dong Z, Gajewska-Knapik K, Kilby MD, Mone F.
    Ultrasound Obstet Gynecol; 2024 Jan 25; 63(1):15-23. PubMed ID: 37725747
    [Abstract] [Full Text] [Related]

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