194 related articles for article (PubMed ID: 33201576)
1. Chromosomal mosaicism detected by karyotyping and chromosomal microarray analysis in prenatal diagnosis.
Zhang Y; Zhong M; Zheng D
J Cell Mol Med; 2021 Jan; 25(1):358-366. PubMed ID: 33201576
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. The difference between karyotype analysis and chromosome microarray for mosaicism of aneuploid chromosomes in prenatal diagnosis.
Hao M; Li L; Zhang H; Li L; Liu R; Yu Y
J Clin Lab Anal; 2020 Dec; 34(12):e23514. PubMed ID: 32864771
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. Application of various genetic analysis techniques for detecting two rare cases of 9p duplication mosaicism during prenatal diagnosis.
Zhang S; Zhou Y; Xiao G; Qiu X
Mol Genet Genomic Med; 2023 Oct; 11(10):e2229. PubMed ID: 37337789
[TBL] [Abstract][Full Text] [Related]
9. Fetal mosaicism, should conventional karyotype always be performed?
Su L; Wu X; Liang B; Lin N; Xie X; Cai M; Zheng L; Wang M; Xu L
J Obstet Gynaecol Res; 2023 Dec; 49(12):2836-2848. PubMed ID: 37844871
[TBL] [Abstract][Full Text] [Related]
10. Validation of a Chromosomal Microarray for Prenatal Diagnosis Using a Prospective Cohort of Pregnancies with Increased Risk for Chromosome Abnormalities.
Wright D; Carey L; Battersby S; Nguyen T; Clarke M; Nash B; Gulesserian E; Cross J; Darmanian A
Genet Test Mol Biomarkers; 2016 Dec; 20(12):791-798. PubMed ID: 27690282
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of fetuses conceived by assisted reproductive technology by karyotyping and chromosomal microarray analysis.
Guo H; Sheng R; Zhang X; Jin X; Gu W; Liu T; Dong H; Jia R
PeerJ; 2023; 11():e14678. PubMed ID: 36684682
[TBL] [Abstract][Full Text] [Related]
12. [The value of chromosomal microarray analysis and fluorescence in situ hybridization for the prenatal diagnosis of chromosomal mosaicisms].
Zheng J; An N; Li M; Xu M; Guan Y; Liu J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 May; 40(5):527-531. PubMed ID: 37102283
[TBL] [Abstract][Full Text] [Related]
13. MCDA twins with discordant malformations: submicroscopic chromosomal anomalies detected by chromosomal microarray analysis and clinical outcomes.
Peng R; Zhou Y; Xie HN; Zheng J; Xie YJ; Yang JB
Prenat Diagn; 2016 Aug; 36(8):766-74. PubMed ID: 27315788
[TBL] [Abstract][Full Text] [Related]
14. Monochorionic twins discordant for mosaic trisomy 14.
He M; Pepperell JR; Gundogan F; De Paepe ME; Maggio L; Lu S; Kostadinov S; O'Brien B; Delamonte S; Pinar H; Tantravahi U
Am J Med Genet A; 2014 May; 164A(5):1227-33. PubMed ID: 24458767
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counselling.
Gilbert B; Yardin C; Briault S; Belin V; Lienhardt A; Aubard Y; Battin J; Servaud M; Philippe HJ; Lacombe D
Prenat Diagn; 2002 Aug; 22(8):697-702. PubMed ID: 12210579
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Prenatal microarray analysis as second-tier diagnostic test: single-center prospective study.
Schmid M; Stary S; Springer S; Bettelheim D; Husslein P; Streubel B
Ultrasound Obstet Gynecol; 2013 Mar; 41(3):267-73. PubMed ID: 23292918
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Discordant circulating fetal DNA and subsequent cytogenetics reveal false negative, placental mosaic, and fetal mosaic cfDNA genotypes.
Lebo RV; Novak RW; Wolfe K; Michelson M; Robinson H; Mancuso MS
J Transl Med; 2015 Aug; 13():260. PubMed ID: 26260800
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]