247 related articles for article (PubMed ID: 33901244)
1. Benefit versus risk of chromosomal microarray analysis performed in pregnancies with normal and positive prenatal screening results: A retrospective study.
Moshonov R; Hod K; Azaria B; Abadi-Korek I; Berger R; Shohat M
PLoS One; 2021; 16(4):e0250734. PubMed ID: 33901244
[TBL] [Abstract][Full Text] [Related]
2. Assessment of Combined Karyotype Analysis and Chromosome Microarray Analysis in Prenatal Diagnosis: A Cohort Study of 3710 Pregnancies.
Wang J; Wang D; Yin Y; Deng Y; Ye M; Wei P; Zhang Z; Chen C; Qin S; Wang X
Genet Res (Camb); 2022; 2022():6791439. PubMed ID: 36636555
[TBL] [Abstract][Full Text] [Related]
3. Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities.
Fiorentino F; Napoletano S; Caiazzo F; Sessa M; Bono S; Spizzichino L; Gordon A; Nuccitelli A; Rizzo G; Baldi M
Eur J Hum Genet; 2013 Jul; 21(7):725-30. PubMed ID: 23211699
[TBL] [Abstract][Full Text] [Related]
4. Role of late amniocentesis in the era of modern genomic technologies.
Daum H; Ben David A; Nadjari M; Zenvirt S; Helman S; Yanai N; Meiner V; Yagel S; Frumkin A; Shkedi Rafid S;
Ultrasound Obstet Gynecol; 2019 May; 53(5):676-685. PubMed ID: 30155922
[TBL] [Abstract][Full Text] [Related]
5. Microarray and RASopathy-disorder testing in fetuses with increased nuchal translucency.
Sinajon P; Chitayat D; Roifman M; Wasim S; Carmona S; Ryan G; Noor A; Kolomietz E; Chong K
Ultrasound Obstet Gynecol; 2020 Mar; 55(3):383-390. PubMed ID: 31115076
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restriction.
Zhu H; Lin S; Huang L; He Z; Huang X; Zhou Y; Fang Q; Luo Y
Prenat Diagn; 2016 Jul; 36(7):686-92. PubMed ID: 27221052
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. [The value of combined use of chromosomal karyotyping and chromosome microarray analysis for prenatal diagnosis].
Rao H; Liu Y; Lu Q; Huang N; Zhou J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Apr; 37(4):392-396. PubMed ID: 32219820
[TBL] [Abstract][Full Text] [Related]
11. Prenatal Diagnosis of Chromosomal Mosaicism in 18,369 Cases of Amniocentesis.
Kang H; Wang L; Xie Y; Chen Y; Gao C; Li X; Hu Y; Liu Q
Am J Perinatol; 2024 May; 41(S 01):e2058-e2068. PubMed ID: 37336233
[TBL] [Abstract][Full Text] [Related]
12. Chromosomal microarray analysis and prenatal diagnosis.
Lo JO; Shaffer BL; Feist CD; Caughey AB
Obstet Gynecol Surv; 2014 Oct; 69(10):613-21. PubMed ID: 25336071
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Prenatal Diagnosis of Talipes Equinovarus by Ultrasound and Chromosomal Microarray Analysis: A Chinese Single-Center Retrospective Study.
Huang R; Yang X; Zhou H; Fu F; Cheng K; Wang Y; Ma C; Li R; Jing X; Han J; Zhen L; Pan M; Li D; Liao C
Genes (Basel); 2022 Sep; 13(9):. PubMed ID: 36140741
[TBL] [Abstract][Full Text] [Related]
15. Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.
Hillman SC; McMullan DJ; Hall G; Togneri FS; James N; Maher EJ; Meller CH; Williams D; Wapner RJ; Maher ER; Kilby MD
Ultrasound Obstet Gynecol; 2013 Jun; 41(6):610-20. PubMed ID: 23512800
[TBL] [Abstract][Full Text] [Related]
16. [Value of detection of cell-free fetal DNA in maternal plasma in the prenatal diagnosis of chromosomal abnormalities].
Wang SJ; Gao ZY; Lu YP; Li YL; You YQ; Zhang LW; Wang LX; Xu H
Zhonghua Fu Chan Ke Za Zhi; 2012 Nov; 47(11):808-12. PubMed ID: 23302119
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Clinical utility of expanded non-invasive prenatal screening and chromosomal microarray analysis in high-risk pregnancy.
Zhu X; Chen M; Wang H; Guo Y; Chau MHK; Yan H; Cao Y; Kwok YKY; Chen J; Hui ASY; Zhang R; Meng Z; Zhu Y; Leung TY; Xiong L; Kong X; Choy KW
Ultrasound Obstet Gynecol; 2021 Mar; 57(3):459-465. PubMed ID: 32198896
[TBL] [Abstract][Full Text] [Related]
19. Diagnostic accuracy and value of chromosomal microarray analysis for chromosomal abnormalities in prenatal detection: A prospective clinical study.
Huang H; Wang Y; Zhang M; Lin N; An G; He D; Chen M; Chen L; Xu L
Medicine (Baltimore); 2021 May; 100(20):e25999. PubMed ID: 34011095
[TBL] [Abstract][Full Text] [Related]
20. Risk factors for procedure-related fetal losses after mid-trimester genetic amniocentesis.
Kong CW; Leung TN; Leung TY; Chan LW; Sahota DS; Fung TY; Lau TK
Prenat Diagn; 2006 Oct; 26(10):925-30. PubMed ID: 16838383
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]