1068 related articles for article (PubMed ID: 25675923)
1. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia.
Chen CP; Wang YL; Chern SR; Liu YP; Peng CR; Kuo YL; Wu PS; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2015 Feb; 54(1):66-70. PubMed ID: 25675923
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism.
Chen CP; Chen YY; Chern SR; Wu PS; Su JW; Chen YT; Lee CC; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2013 Sep; 52(3):395-400. PubMed ID: 24075380
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16.
Chen CP; Ko TM; Chern SR; Wu PS; Chen SW; Lai ST; Yang CW; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Aug; 56(4):545-549. PubMed ID: 28805616
[TBL] [Abstract][Full Text] [Related]
4. Low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with cytogenetic discrepancy in various tissues, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcome.
Chen CP; Wu FT; Pan YT; Wu PS; Chen WL; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2023 Nov; 62(6):891-895. PubMed ID: 38008510
[TBL] [Abstract][Full Text] [Related]
5. High-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with positive NIPT for trisomy 21, prenatal progressive decrease of the trisomy 21 cell line, acute fatty liver of pregnancy and intrauterine fetal death in late gestation.
Chen CP; Wang LK; Wu FT; Pan YT; Wu PS; Chen WL; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2023 Nov; 62(6):896-900. PubMed ID: 38008511
[TBL] [Abstract][Full Text] [Related]
6. Low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcome.
Chen CP; Wu FT; Pan YT; Wu PS; Lee CC; Chiu CL; Wang W
Taiwan J Obstet Gynecol; 2024 May; 63(3):394-397. PubMed ID: 38802205
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy.
Chen CP; Chern SR; Wang LK; Wu PS; Wu FT; Chen YY; Town DD; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2020 Nov; 59(6):938-940. PubMed ID: 33218416
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital heart defects.
Chen CP; Huang JP; Chen SW; Chern SR; Wu PS; Wu FT; Chen WL; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2020 Jan; 59(1):135-139. PubMed ID: 32039782
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of maternal uniparental disomy 21 in association with low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome.
Chen CP; Liou JD; Chern SR; Wu PS; Chen SW; Wu FT; Lee MS; Chen YY; Wang W
Taiwan J Obstet Gynecol; 2022 Jan; 61(1):146-149. PubMed ID: 35181027
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes.
Chen CP; Wang YL; Chern SR; Wu PS; Chen YN; Chen SW; Chen LF; Lee MS; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Apr; 55(2):285-7. PubMed ID: 27125416
[TBL] [Abstract][Full Text] [Related]
12. Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis.
Chen CP; Su YN; Su JW; Chern SR; Chen YT; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2013 Mar; 52(1):97-105. PubMed ID: 23548227
[TBL] [Abstract][Full Text] [Related]
13. Second-trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature.
Chen CP; Chern SR; Cheng SJ; Chang TY; Yeh LF; Lee CC; Pan CW; Wang W; Tzen CY
Prenat Diagn; 2004 Jun; 24(6):455-62. PubMed ID: 15229846
[TBL] [Abstract][Full Text] [Related]
14. Trisomy 7 mosaicism at amniocentesis: interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism.
Chen CP; Huang HK; Su YN; Chern SR; Su JW; Lee CC; Town DD; Chen WL; Chen YT; Wang W
Taiwan J Obstet Gynecol; 2012 Mar; 51(1):77-82. PubMed ID: 22482973
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus.
Chen CP; Ko TM; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Town DD; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2021 May; 60(3):534-539. PubMed ID: 33966743
[TBL] [Abstract][Full Text] [Related]
16. Mosaic trisomy 16 at amniocentesis in a pregnancy associated with positive non-invasive prenatal testing for trisomy 16, placental trisomy 16, intrauterine growth restriction, intrauterine fetal death, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, and prenatal progressive decrease of the aneuploid cell line.
Chen CP; Wu FT; Chen YY; Pan YT; Wu PS; Lee MS; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2023 Jul; 62(4):597-601. PubMed ID: 37407203
[TBL] [Abstract][Full Text] [Related]
17. Low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the aneuploid cell line and a favorable fetal outcome.
Chen CP; Wu FT; Pan YT; Wu PS; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2023 Nov; 62(6):910-914. PubMed ID: 38008514
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of mosaicism for double aneuploidy of 47,XXY and trisomy 7 (48,XXY,+7) at amniocentesis in a pregnancy with a favorable outcome.
Chen CP; Tsai HT; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Town DD; Chen WL; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2021 May; 60(3):543-548. PubMed ID: 33966745
[TBL] [Abstract][Full Text] [Related]
19. Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis.
Chen CP; Hsu TY; Ko TM; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Lee CC; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2020 Sep; 59(5):728-735. PubMed ID: 32917326
[TBL] [Abstract][Full Text] [Related]
20. Rapid diagnosis of pseudomosaicism in a case of Level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amniocentesis.
Chen CP; Chang SJ; Chern SR; Wu PS; Chen YN; Chen SW; Yang CW; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2016 Aug; 55(4):602-3. PubMed ID: 27590391
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
