131 related articles for article (PubMed ID: 37336233)
1. 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]
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. [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]
4. [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]
5. Limited additional value of karyotyping cultured amniotic fluid cell colonies in addition to microarray on uncultured cells for confirmation of abnormal non-invasive prenatal testing results.
Donze SH; Srebniak MI; Diderich KEM; van den Born M; Galjaard RJ; Govaerts LCP; van der Schoot V; Knapen MFCM; Joosten M; Van Opstal D
Prenat Diagn; 2024 Apr; 44(4):401-408. PubMed ID: 38141050
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of a trisomy 7 mosaic case: CMA, CNV-seq, karyotyping, interphase FISH, and MS-MLPA, which technique to choose?
Cong X; Zhang T; Li Z; Luo X; Hu L; Liu W
BMC Pregnancy Childbirth; 2024 May; 24(1):338. PubMed ID: 38702634
[TBL] [Abstract][Full Text] [Related]
7. Mosaic isochromosome 20q at amniocentesis: Prenatal diagnosis, genetic counseling and literature review.
Chen CP; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Wang W
Taiwan J Obstet Gynecol; 2019 Nov; 58(6):855-858. PubMed ID: 31759542
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [Prenatal diagnosis of monochorionic-diamniotic twins discordant for 45,X/46,XX mosaicism].
Hu J; Xi H; Ma N; Pang J; Luo Y; Jia Z; Wang H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Mar; 36(3):260-262. PubMed ID: 30835360
[TBL] [Abstract][Full Text] [Related]
10. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].
Zhang YP; Wu JP; Li XT; Lei CX; Xu JZ; Yin M
Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):644-8. PubMed ID: 22176986
[TBL] [Abstract][Full Text] [Related]
11. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].
Ulmer R; Pfeiffer RA; Kollert A; Beinder E
Z Geburtshilfe Neonatol; 2000; 204(1):1-7. PubMed ID: 10721179
[TBL] [Abstract][Full Text] [Related]
12. Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister-Killian syndrome.
Chen CP; Peng CR; Chern SR; Kuo YL; Wu PS; Town DD; Pan CW; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2014 Dec; 53(4):566-71. PubMed ID: 25510702
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of BACs-on-Beads assay in 1520 cases from Fujian Province, China.
Wang Y; Zhang M; Chen L; Huang H; Xu L
Mol Genet Genomic Med; 2020 Oct; 8(10):e1446. PubMed ID: 32767744
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Prenatal diagnosis of mosaic trisomy 18 and maternal uniparental disomy 18 by amniocentesis in a pregnancy associated with cytogenetic discrepancy in various tissues and a favorable fetal outcome.
Chen CP; Wu FT; Pan YT; Chern SR; Wu PS; Chiu CL; Lee CC; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2023 Jul; 62(4):606-610. PubMed ID: 37407205
[TBL] [Abstract][Full Text] [Related]
16. Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review.
Chen CP; Chern SR; Chen YN; Wu PS; Yang CW; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2015 Aug; 54(4):426-31. PubMed ID: 26384064
[TBL] [Abstract][Full Text] [Related]
17. Interphase fluorescence in situ hybridization assisting in prenatal counseling for amniocentesis karyotyping-detected fetal mosaicism.
Su SY; Chueh HY; Li CP; Chang YL; Chang SD; Chen CP
Taiwan J Obstet Gynecol; 2015 Oct; 54(5):588-91. PubMed ID: 26522116
[TBL] [Abstract][Full Text] [Related]
18. [Combined chromosomal microarray analysis and fluorescence in situ hybridization for prenatal diagnosis of two cases with Pallister-Killian syndrome].
Wang T; Ren C; Guo L; Lu J; Chen H; Huang H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Jun; 36(6):571-573. PubMed ID: 31055807
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Perinatal detection of disomy X cell line by fluorescence in situ hybridization in a pregnancy with 45,X/47,XXX at amniocentesis, cytogenetic discrepancy in various tissues and a favorable outcome.
Chen CP; Wu FT; Pan YT; Wu PS; Chen WL; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2023 Nov; 62(6):906-909. PubMed ID: 38008513
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]