248 related articles for article (PubMed ID: 32632923)
1. Chromosome microarray analysis should be offered to all invasive prenatal diagnostic testing following a normal rapid aneuploidy test result.
Rodriguez-Revenga L; Madrigal I; Borrell A; Martinez JM; Sabria J; Martin L; Jimenez W; Mira A; Badenas C; Milà M
Clin Genet; 2020 Oct; 98(4):379-383. PubMed ID: 32632923
[TBL] [Abstract][Full Text] [Related]
2. 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; 162(7):354-364. PubMed ID: 36907182
[TBL] [Abstract][Full Text] [Related]
3. Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
Wang J; Chen L; Zhou C; Wang L; Xie H; Xiao Y; Zhu H; Hu T; Zhang Z; Zhu Q; Liu Z; Liu S; Wang H; Xu M; Ren Z; Yu F; Cram DS; Liu H
Am J Obstet Gynecol; 2018 Sep; 219(3):287.e1-287.e18. PubMed ID: 29852155
[TBL] [Abstract][Full Text] [Related]
4. Population-based trends in invasive prenatal diagnosis for ultrasound-based indications: two decades of change from 1994 to 2016.
Lostchuck E; Poulton A; Halliday J; Hui L
Ultrasound Obstet Gynecol; 2019 Apr; 53(4):503-511. PubMed ID: 29877030
[TBL] [Abstract][Full Text] [Related]
5. Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomalies.
Li L; He Z; Huang X; Lin S; Wu J; Huang L; Wan Y; Fang Q
Ultrasound Obstet Gynecol; 2020 Apr; 55(4):502-509. PubMed ID: 30977228
[TBL] [Abstract][Full Text] [Related]
6. Clinical utility of expanded non-invasive prenatal screening compared with chromosomal microarray analysis in over 8000 pregnancies without major structural anomaly.
Maya I; Salzer Sheelo L; Brabbing-Goldstein D; Matar R; Kahana S; Agmon-Fishman I; Klein C; Gurevitch M; Basel-Salmon L; Sagi-Dain L
Ultrasound Obstet Gynecol; 2023 Jun; 61(6):698-704. PubMed ID: 36776119
[TBL] [Abstract][Full Text] [Related]
7. Application of chromosome microarray analysis in prenatal diagnosis.
Xia M; Yang X; Fu J; Teng Z; Lv Y; Yu L
BMC Pregnancy Childbirth; 2020 Nov; 20(1):696. PubMed ID: 33198662
[TBL] [Abstract][Full Text] [Related]
8. Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies.
Sagi-Dain L; Cohen Vig L; Kahana S; Yacobson S; Tenne T; Agmon-Fishman I; Klein C; Matar R; Basel-Salmon L; Maya I
Genet Med; 2019 Nov; 21(11):2462-2467. PubMed ID: 31123319
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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; 41(4):375-82. PubMed ID: 23233332
[TBL] [Abstract][Full Text] [Related]
11. Detection of copy number variants using chromosomal microarray analysis for the prenatal diagnosis of congenital heart defects with normal karyotype.
Song T; Wan S; Li Y; Xu Y; Dang Y; Zheng Y; Li C; Zheng J; Chen B; Zhang J
J Clin Lab Anal; 2019 Jan; 33(1):e22630. PubMed ID: 30047171
[TBL] [Abstract][Full Text] [Related]
12. The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies.
Srebniak MI; Knapen MFCM; Polak M; Joosten M; Diderich KEM; Govaerts LCP; Boter M; Kromosoeto JNR; van Hassel DACM; Huijbregts G; van IJcken WFJ; Heydanus R; Dijkman A; Toolenaar T; de Vries FAT; Knijnenburg J; Go ATJI; Galjaard RH; Van Opstal D
Hum Mutat; 2017 Jul; 38(7):880-888. PubMed ID: 28409863
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. The application of chromosomal microarray analysis to the prenatal diagnosis of isolated mild ventriculomegaly.
Duan HL; Zhu XY; Zhu YJ; Wu X; Zhao GF; Wang WJ; Li J
Taiwan J Obstet Gynecol; 2019 Mar; 58(2):251-254. PubMed ID: 30910148
[TBL] [Abstract][Full Text] [Related]
15. The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings.
Hui AS; Chau MHK; Chan YM; Cao Y; Kwan AH; Zhu X; Kwok YK; Chen Z; Lao TT; Choy KW; Leung TY
Acta Obstet Gynecol Scand; 2021 Feb; 100(2):235-243. PubMed ID: 32981064
[TBL] [Abstract][Full Text] [Related]
16. Isolated fetal horseshoe kidney does not seem to increase the risk for abnormal chromosomal microarray results.
Sagi-Dain L; Maya I; Falik-Zaccai T; Feingold-Zadok M; Lev D; Yonath H; Kaliner E; Frumkin A; Ben Shachar S; Singer A
Eur J Obstet Gynecol Reprod Biol; 2018 Mar; 222():80-83. PubMed ID: 29367169
[TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of fetuses with increased nuchal translucency using an approach based on quantitative fluorescent polymerase chain reaction and genomic microarray.
Pan M; Han J; Zhen L; Yang X; Li R; Liao C; Li DZ
Eur J Obstet Gynecol Reprod Biol; 2016 Feb; 197():164-7. PubMed ID: 26771907
[TBL] [Abstract][Full Text] [Related]
18. Fetal hydrops and the Incremental yield of Next-generation sequencing over standard prenatal Diagnostic testing (FIND) study: prospective cohort study and meta-analysis.
Mone F; Eberhardt RY; Hurles ME; Mcmullan DJ; Maher ER; Lord J; Chitty LS; Dempsey E; Homfray T; Giordano JL; Wapner RJ; Sun L; Sparks TN; Norton ME; Kilby MD
Ultrasound Obstet Gynecol; 2021 Oct; 58(4):509-518. PubMed ID: 33847422
[TBL] [Abstract][Full Text] [Related]
19. Chromosome microarray analysis combined with karyotype analysis is a powerful tool for the detection in pregnant women with high-risk indicators.
Qian G; Cai L; Yao H; Dong X
BMC Pregnancy Childbirth; 2023 Nov; 23(1):784. PubMed ID: 37951870
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis by chromosomal microarray analysis.
Levy B; Wapner R
Fertil Steril; 2018 Feb; 109(2):201-212. PubMed ID: 29447663
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
