284 related articles for article (PubMed ID: 34304437)
1. [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; 56(7):458-466. PubMed ID: 34304437
[No Abstract] [Full Text] [Related]
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;
Lancet; 2019 Feb; 393(10173):747-757. PubMed ID: 30712880
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [Prospective cohort study of fetal nuchal translucency in first-trimester and pregnancy outcome].
Tang HR; Zhang Y; Ru T; Li J; Yang L; Xu Y; Duan HL; Wang Y; Wang Y; Hu YL; Zhang Y; Zheng MM
Zhonghua Fu Chan Ke Za Zhi; 2020 Feb; 55(2):94-99. PubMed ID: 32146737
[No Abstract] [Full Text] [Related]
5. Prenatal whole-exome sequencing in fetuses with increased nuchal translucency.
Cao C; Liu F; Yang Y; Zhang Q; Huang J; Liu X
Mol Genet Genomic Med; 2023 Nov; 11(11):e2246. PubMed ID: 37766479
[TBL] [Abstract][Full Text] [Related]
6. 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; 62(1):94-105. PubMed ID: 36779229
[TBL] [Abstract][Full Text] [Related]
7. Genetic Examination for Fetuses with Increased Fetal Nuchal Translucency by Genomic Technology.
Xue S; Yan H; Chen J; Li N; Wang J; Liu Y; Zhang H; Li S; Zhang W; Chen D; Chen M
Cytogenet Genome Res; 2020; 160(2):57-62. PubMed ID: 32036363
[TBL] [Abstract][Full Text] [Related]
8. [Comparison of results of prenatal diagnosis by different techniques for fetuses with increased nuchal translucency].
Dai W; Liu X; Ma X; Yu Z; Li H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 May; 40(5):532-537. PubMed ID: 37102284
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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; 16(1):262. PubMed ID: 37880672
[TBL] [Abstract][Full Text] [Related]
11. 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; 393(10173):758-767. PubMed ID: 30712878
[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. Importance of complete phenotyping in prenatal whole exome sequencing.
Aarabi M; Sniezek O; Jiang H; Saller DN; Bellissimo D; Yatsenko SA; Rajkovic A
Hum Genet; 2018 Feb; 137(2):175-181. PubMed ID: 29392406
[TBL] [Abstract][Full Text] [Related]
14. [Analysis of copy number variation by CMA in fetus with increased nuchal translucency].
Du L; Xie HN; Zheng J; He M
Zhonghua Fu Chan Ke Za Zhi; 2018 Oct; 53(10):671-676. PubMed ID: 30369122
[No Abstract] [Full Text] [Related]
15. 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; 23(1):577. PubMed ID: 37980516
[TBL] [Abstract][Full Text] [Related]
16. Fetal exome sequencing for isolated increased nuchal translucency: should we be doing it?
Mellis R; Eberhardt RY; Hamilton SJ; ; McMullan DJ; Kilby MD; Maher ER; Hurles ME; Giordano JL; Aggarwal V; Goldstein DB; Wapner RJ; Chitty LS
BJOG; 2022 Jan; 129(1):52-61. PubMed ID: 34411415
[TBL] [Abstract][Full Text] [Related]
17. Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype.
Su L; Huang H; An G; Cai M; Wu X; Li Y; Xie X; Lin Y; Wang M; Xu L
Mol Genet Genomic Med; 2019 Aug; 7(8):e811. PubMed ID: 31209990
[TBL] [Abstract][Full Text] [Related]
18. Pathologic whole exome sequencing analysis in fetuses with minor sonographic abnormal findings and normal chromosomal microarray analysis: case series.
Achiron R; Kassif E; Shohat M; Kivilevitch Z
J Matern Fetal Neonatal Med; 2022 Dec; 35(25):9730-9735. PubMed ID: 35282760
[TBL] [Abstract][Full Text] [Related]
19. Whole Genome Sequencing in the Evaluation of Fetal Structural Anomalies: A Parallel Test with Chromosomal Microarray Plus Whole Exome Sequencing.
Zhou J; Yang Z; Sun J; Liu L; Zhou X; Liu F; Xing Y; Cui S; Xiong S; Liu X; Yang Y; Wei X; Zou G; Wang Z; Wei X; Wang Y; Zhang Y; Yan S; Wu F; Zeng F; Wang J; Duan T; Peng Z; Sun L
Genes (Basel); 2021 Mar; 12(3):. PubMed ID: 33800913
[TBL] [Abstract][Full Text] [Related]
20. [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; 54(4):221-225. PubMed ID: 31006186
[No Abstract] [Full Text] [Related]
[Next] [New Search]