These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
158 related articles for article (PubMed ID: 38189110)
1. Prenatal diagnosis and outcomes in fetuses with duplex kidney. Ma C; Huang R; Fu F; Zhou H; Wang Y; Yan S; Guo F; Chen H; Li L; Jing X; Li F; Han J; Li D; Li R; Liao C Int J Gynaecol Obstet; 2024 Jul; 166(1):353-359. PubMed ID: 38189110 [TBL] [Abstract][Full Text] [Related]
2. Association of prenatal renal ultrasound abnormalities with pathogenic copy number variants in a large Chinese cohort. Su J; Qin Z; Fu H; Luo J; Huang Y; Huang P; Zhang S; Liu T; Lu W; Li W; Jiang T; Wei S; Yang S; Shen Y Ultrasound Obstet Gynecol; 2022 Feb; 59(2):226-233. PubMed ID: 34090309 [TBL] [Abstract][Full Text] [Related]
3. Molecular diagnostic in fetuses with isolated congenital anomalies of the kidney and urinary tract by whole-exome sequencing. Zhou X; Wang Y; Shao B; Wang C; Hu P; Qiao F; Xu Z J Clin Lab Anal; 2020 Nov; 34(11):e23480. PubMed ID: 32779812 [TBL] [Abstract][Full Text] [Related]
4. 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; 40(10):1290-1299. PubMed ID: 32436246 [TBL] [Abstract][Full Text] [Related]
5. Genetic diagnosis of common fetal renal abnormalities detected on prenatal ultrasound. Liu L; Li J; Li Y; Li H; Yang B; Fan H; Wang J; Gu Y; Yu H; Bai M; Yu T; Cui S; Cheng G; Ren C Prenat Diagn; 2022 Jun; 42(7):894-900. PubMed ID: 35478332 [TBL] [Abstract][Full Text] [Related]
6. Exome sequencing as first-tier test for fetuses with severe central nervous system structural anomalies. Yaron Y; Ofen Glassner V; Mory A; Zunz Henig N; Kurolap A; Bar Shira A; Brabbing Goldstein D; Marom D; Ben Sira L; Baris Feldman H; Malinger G; Krajden Haratz K; Reches A Ultrasound Obstet Gynecol; 2022 Jul; 60(1):59-67. PubMed ID: 35229910 [TBL] [Abstract][Full Text] [Related]
7. Optimal prenatal genetic diagnostic approach for posterior fossa malformation: karyotyping, copy number variant testing, or whole-exome sequencing? Juan Z; Cuixia G; Yuanjie C; Yan L; Ling Y; Tiejuan Z; Li W; Jijing H; Guohui Z; Yousheng Y; Qingqing W; Lijuan S Eur J Med Res; 2024 Jul; 29(1):397. PubMed ID: 39085968 [TBL] [Abstract][Full Text] [Related]
8. 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; 58(3):377-387. PubMed ID: 33142350 [TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencing. Huang R; Fu F; Zhou H; Zhang L; Lei T; Cheng K; Yan S; Guo F; Wang Y; Ma C; Li R; Yu Q; Deng Q; Li L; Yang X; Han J; Li D; Liao C Hum Genet; 2023 Jun; 142(6):835-847. PubMed ID: 37095353 [TBL] [Abstract][Full Text] [Related]
10. [Whole exome sequencing analysis of 37 fetuses with cardiac abnormalities]. Xu X; Ye F; Zhang J; Jin K; Shen Q; Shen S; Jin F Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Aug; 41(8):903-908. PubMed ID: 39097270 [TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in fetuses with ultrasound anomalies in the urinary system. Hu T; Zhang Z; Wang J; Li Q; Zhu H; Lai Y; Wang H; Liu S Prenat Diagn; 2019 Nov; 39(12):1096-1106. PubMed ID: 31461547 [TBL] [Abstract][Full Text] [Related]
12. [Prenatal genetic diagnosis of the fetuses with isolated corpus callosum abnormality]. She Q; Zhen L; Fu F; Lei TY; Li LS; Li R; Wang D; Zhang YL; Jing XY; Yi CX; Zhong HZ; Tan WH; Li FG; Liao C Zhonghua Fu Chan Ke Za Zhi; 2022 Sep; 57(9):671-677. PubMed ID: 36177578 [No Abstract] [Full Text] [Related]
13. Spectrum of congenital anomalies of the kidney and urinary tract (CAKUT) including renal parenchymal malformations during fetal life and the implementation of prenatal exome sequencing (WES). Koenigbauer JT; Fangmann L; Reinhardt C; Weichert A; Henrich W; Saskia B; Gabriel HP Arch Gynecol Obstet; 2024 Jun; 309(6):2613-2622. PubMed ID: 37535131 [TBL] [Abstract][Full Text] [Related]
14. 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; 51(4):493-502. PubMed ID: 28976722 [TBL] [Abstract][Full Text] [Related]
15. Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing. Shi X; Tang H; Lu J; Yang X; Ding H; Wu J Ann Med; 2021 Dec; 53(1):1285-1291. PubMed ID: 34374610 [TBL] [Abstract][Full Text] [Related]
16. 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; Lancet; 2019 Feb; 393(10173):747-757. PubMed ID: 30712880 [TBL] [Abstract][Full Text] [Related]
17. 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; 36(1):2193285. PubMed ID: 37019452 [TBL] [Abstract][Full Text] [Related]
18. Prenatal genetic testing in 19 fetuses with corpus callosum abnormality. She Q; Tang E; Peng C; Wang L; Wang D; Tan W J Clin Lab Anal; 2021 Nov; 35(11):e23971. PubMed ID: 34569664 [TBL] [Abstract][Full Text] [Related]
19. Prenatal exome sequencing analysis in fetuses with central nervous system anomalies. Zhi Y; Liu L; Wang H; Chen X; Lv Y; Cui X; Chang H; Wang Y; Cui S Ultrasound Obstet Gynecol; 2023 Nov; 62(5):721-726. PubMed ID: 37204857 [TBL] [Abstract][Full Text] [Related]
20. Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center. Xue H; Yu A; Chen L; Guo Q; Zhang L; Lin N; Chen X; Xu L; Huang H Sci Rep; 2024 Jul; 14(1):16266. PubMed ID: 39009665 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]