940 related articles for article (PubMed ID: 23040927)
21. Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis in a pregnancy with a favorable outcome.
Chen CP; Ko TM; Chen TC; Chern SR; Wu PS; Chen SW; Wu FT; Chen WL; Chen YY; Wang W
Taiwan J Obstet Gynecol; 2022 Jul; 61(4):677-683. PubMed ID: 35779921
[TBL] [Abstract][Full Text] [Related]
22. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.
Chen CP; Chen M; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chang SP; Yang CW; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Aug; 56(4):527-533. PubMed ID: 28805612
[TBL] [Abstract][Full Text] [Related]
23. Prenatal diagnosis of mosaic tetrasomy 18p.
Chen CP; Ko TM; Su YN; Chern SR; Su JW; Chen YT; Town DD; Wang W
Taiwan J Obstet Gynecol; 2012 Dec; 51(4):625-9. PubMed ID: 23276569
[TBL] [Abstract][Full Text] [Related]
24. Mosaic tetrasomy 9p at amniocentesis in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the aneuploid cell line and cytogenetic discrepancy in various tissues.
Chen CP; Chen SW; Chern SR; Wu PS; Wu FT; Pan YT; Lee CC; Pan CW; Chen YY; Wang W
Taiwan J Obstet Gynecol; 2023 Jan; 62(1):148-154. PubMed ID: 36720529
[TBL] [Abstract][Full Text] [Related]
25. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from inv dup(15).
Chen CP; Lin HY; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Fran S; Chen YY; Town DD; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2020 Jul; 59(4):580-585. PubMed ID: 32653133
[TBL] [Abstract][Full Text] [Related]
26. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome.
Chen CP; Ko TM; Chen YY; Su JW; Wang W
Gene; 2013 Sep; 527(1):384-8. PubMed ID: 23747353
[TBL] [Abstract][Full Text] [Related]
27. Low-level mosaic trisomy 2 at amniocentesis in a pregnancy associated with positive NIPT and CVS results for trisomy 2, maternal uniparental disomy 2, perinatal progressive decrease of the aneuploid cell line, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, intrauterine growth restriction and a favorable fetal outcome.
Chen CP; Wu FT; Chern SR; Wu PS; Pan YT; Lee CC; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2023 Jul; 62(4):571-576. PubMed ID: 37407197
[TBL] [Abstract][Full Text] [Related]
28. Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis in a pregnancy with a favorable outcome.
Chen CP; Lin YH; Wu PS; Chern SR; Chen SW; Wu FT; Lee CC; Pan CW; Chen YY; Wang W
Taiwan J Obstet Gynecol; 2022 Jan; 61(1):138-140. PubMed ID: 35181025
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review.
Chen CP; Chen M; Wu CH; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Chang SP; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2017 Aug; 56(4):554-557. PubMed ID: 28805618
[TBL] [Abstract][Full Text] [Related]
31. Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality.
Chen CP; Chern SR; Chen YN; Chen SW; Wu PS; Yang CW; Lee CC; Lee MS; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Apr; 56(2):217-223. PubMed ID: 28420511
[TBL] [Abstract][Full Text] [Related]
32. Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay.
Chen CP; Chiang S; Wang KL; Cho FN; Chen M; Chern SR; Wu PS; Chen YN; Chen SW; Chang SP; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2016 Jun; 55(3):419-22. PubMed ID: 27343327
[TBL] [Abstract][Full Text] [Related]
33. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome.
Chen CP; Chan CH; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2021 Jan; 60(1):152-156. PubMed ID: 33494992
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.
Chen CP; Chen M; Ko TM; Ma GC; Tsai FJ; Tsai MS; Wu PC; Lee CC; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2010 Dec; 49(4):500-5. PubMed ID: 21199754
[TBL] [Abstract][Full Text] [Related]
36. Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review.
Chen CP; Wang LK; Chern SR; Chen YN; Chen SW; Wu PS; Town DD; Pan CW; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Oct; 55(5):712-717. PubMed ID: 27751421
[TBL] [Abstract][Full Text] [Related]
37. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis.
Chen CP; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2017 Dec; 56(6):852-856. PubMed ID: 29241934
[TBL] [Abstract][Full Text] [Related]
40. Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis.
Chen CP; Su YN; Chern SR; Chen YT; Wu PS; Su JW; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2012 Dec; 51(4):603-11. PubMed ID: 23276565
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
