351 related articles for article (PubMed ID: 26275891)
1. Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities.
Drury S; Williams H; Trump N; Boustred C; ; Lench N; Scott RH; Chitty LS
Prenat Diagn; 2015 Oct; 35(10):1010-7. PubMed ID: 26275891
[TBL] [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 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; 32(10):1665-1675. PubMed ID: 28387813
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Fetal exome sequencing: yield and limitations in a tertiary referral center.
Daum H; Meiner V; Elpeleg O; Harel T;
Ultrasound Obstet Gynecol; 2019 Jan; 53(1):80-86. PubMed ID: 29947050
[TBL] [Abstract][Full Text] [Related]
6. Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomalies.
Alamillo CL; Powis Z; Farwell K; Shahmirzadi L; Weltmer EC; Turocy J; Lowe T; Kobelka C; Chen E; Basel D; Ashkinadze E; D'Augelli L; Chao E; Tang S
Prenat Diagn; 2015 Nov; 35(11):1073-8. PubMed ID: 26147564
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. Molecular autopsy by trio exome sequencing (ES) and postmortem examination in fetuses and neonates with prenatally identified structural anomalies.
Quinlan-Jones E; Lord J; Williams D; Hamilton S; Marton T; Eberhardt RY; Rinck G; Prigmore E; Keelagher R; McMullan DJ; Maher ER; Hurles ME; Kilby MD
Genet Med; 2019 May; 21(5):1065-1073. PubMed ID: 30293990
[TBL] [Abstract][Full Text] [Related]
9. Exome sequencing improves genetic diagnosis of fetal increased nuchal translucency.
Yang X; Huang LY; Pan M; Xu LL; Zhen L; Han J; Li DZ
Prenat Diagn; 2020 Oct; 40(11):1426-1431. PubMed ID: 32668055
[TBL] [Abstract][Full Text] [Related]
10. Rapid prenatal diagnosis using targeted exome sequencing: a cohort study to assess feasibility and potential impact on prenatal counseling and pregnancy management.
Chandler N; Best S; Hayward J; Faravelli F; Mansour S; Kivuva E; Tapon D; Male A; DeVile C; Chitty LS
Genet Med; 2018 Nov; 20(11):1430-1437. PubMed ID: 29595812
[TBL] [Abstract][Full Text] [Related]
11. [Application of chromosomal microarray analysis in prenatal diagnosis of fetuses with increased nuchal translucency].
Ni M; Li J; Zhu X; Zhu Y; Gu L; Wu X; Yang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct; 36(10):970-974. PubMed ID: 31598938
[TBL] [Abstract][Full Text] [Related]
12. Diagnostic yield of next-generation sequencing in fetuses with isolated increased nuchal translucency: systematic review and meta-analysis.
Pauta M; Martinez-Portilla RJ; Borrell A
Ultrasound Obstet Gynecol; 2022 Jan; 59(1):26-32. PubMed ID: 34309942
[TBL] [Abstract][Full Text] [Related]
13. Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges.
Vora NL; Powell B; Brandt A; Strande N; Hardisty E; Gilmore K; Foreman AKM; Wilhelmsen K; Bizon C; Reilly J; Owen P; Powell CM; Skinner D; Rini C; Lyerly AD; Boggess KA; Weck K; Berg JS; Evans JP
Genet Med; 2017 Nov; 19(11):1207-1216. PubMed ID: 28518170
[TBL] [Abstract][Full Text] [Related]
14. A single center experience of prenatal parent-fetus trio exome sequencing for pregnancies with congenital anomalies.
Dufke A; Hoopmann M; Waldmüller S; Prodan NC; Beck-Wödl S; Grasshoff U; Heinrich T; Riess A; Kehrer M; Falb RJ; Liebmann A; Roggia C; Stampfer M; Schadeck M; Müller AJ; Grimmel M; Stöbe P; Gauck D; Buchert-Lo R; Baumann S; Schäferhoff K; Bertrand M; Menden B; Sturm M; Schütz L; Riess O; Ossowski S; Haack TB; Kagan KO
Prenat Diagn; 2022 Jun; 42(7):901-910. PubMed ID: 35574990
[TBL] [Abstract][Full Text] [Related]
15. 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; 40(8):972-983. PubMed ID: 32333414
[TBL] [Abstract][Full Text] [Related]
16. High rate of abnormal findings in Prenatal Exome Trio in low risk pregnancies and apparently normal fetuses.
Vaknin N; Azoulay N; Tsur E; Tripolszki K; Urzi A; Rolfs A; Bauer P; Achiron R; Lipitz S; Goldberg Y; Berger R; Shohat M
Prenat Diagn; 2022 May; 42(6):725-735. PubMed ID: 34918830
[TBL] [Abstract][Full Text] [Related]
17. Committee Opinion No.682: Microarrays and Next-Generation Sequencing Technology: The Use of Advanced Genetic Diagnostic Tools in Obstetrics and Gynecology.
Committee on Genetics and the Society for Maternal-Fetal Medicine
Obstet Gynecol; 2016 Dec; 128(6):e262-e268. PubMed ID: 27875474
[TBL] [Abstract][Full Text] [Related]
18. Comprehensive prenatal diagnostics: Exome versus genome sequencing.
Miceikaite I; Fagerberg C; Brasch-Andersen C; Torring PM; Kristiansen BS; Hao Q; Sperling L; Ibsen MH; Löser K; Bendsen EA; Ousager LB; Larsen MJ
Prenat Diagn; 2023 Aug; 43(9):1132-1141. PubMed ID: 37355983
[TBL] [Abstract][Full Text] [Related]
19. Neu-Laxova syndrome presenting prenatally with increased nuchal translucency and cystic hygroma: The utility of exome sequencing in deciphering the diagnosis.
Bourque DK; Cloutier M; Kernohan KD; Bareke E; Grynspan D; Michaud J; ; Boycott KM
Am J Med Genet A; 2019 May; 179(5):813-816. PubMed ID: 30838783
[TBL] [Abstract][Full Text] [Related]
20. 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(1):25. PubMed ID: 36797717
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
