446 related articles for article (PubMed ID: 27343327)
21. Mosaic distal 10q deletion or 46,XY,del(10) (q26.13)/46,XY at amniocentesis and cordocentesis 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; Wang LK; Wu FT; Pan YT; Wu PS; Lee CC; Chen WL; Chiu CL; Wang W
Taiwan J Obstet Gynecol; 2024 May; 63(3):398-401. PubMed ID: 38802206
[TBL] [Abstract][Full Text] [Related]
22. Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review.
Chen CP; Chen M; Pan YJ; Su YN; Chern SR; Tsai FJ; Chen YT; Wang W
Taiwan J Obstet Gynecol; 2011 Sep; 50(3):331-8. PubMed ID: 22030049
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Prenatal diagnosis and molecular cytogenetic characterization of a familial small supernumerary marker chromosome derived from the acrocentric chromosome 14/22.
Chen CP; Chen M; Ma GC; Chang SP; Chern SR; Chen SW; Wu FT; Chen WL; Lee MS; Chen YY; Wang W
Taiwan J Obstet Gynecol; 2022 Mar; 61(2):364-367. PubMed ID: 35361403
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis.
Chen CP; Su JW; Chern SR; Kuo YL; Wu PS; Lee MS; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2015 Feb; 54(1):58-61. PubMed ID: 25675921
[TBL] [Abstract][Full Text] [Related]
27. Mosaic 46,XY,der(15)t(6;15)(q25.1;p12)/46,XY at amniocentesis in a pregnancy associated with a favorable fetal outcome and postnatal decrease of the aneuploid cell line with the unbalanced translocation.
Chen CP; Chen SW; Chen YY; Chern SR; Wu PS; Wu FT; Pan YT; Lee CC; Chen YY; Wang W
Taiwan J Obstet Gynecol; 2023 Jan; 62(1):142-147. PubMed ID: 36720528
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. 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]
31. 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]
32. Molecular cytogenetic characterization of a de novo small supernumerary marker chromosome derived from chromosome 15 in a pregnancy with incidental detection of a maternal Robertsonian translocation of 45,XX,der(13;14) (q10;q10).
Chen CP; Chen M; Ma GC; Chang SP; Chern SR; Chen SW; Wu FT; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2022 Jan; 61(1):132-134. PubMed ID: 35181023
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Mosaic 46,XY,dup(14) (q12q22.3)/46, XY at amniocentesis in a pregnancy associated with a favorable fetal outcome and cytogenetic discrepancy in various tissues.
Chen CP; Wu FT; Chen CY; Chen SW; Chern SR; Wu PS; Pan YT; Lee CC; Lee MS; Chen YY; Wang W
Taiwan J Obstet Gynecol; 2023 Mar; 62(2):343-347. PubMed ID: 36965906
[TBL] [Abstract][Full Text] [Related]
35. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability.
Chen CP; Lin SP; Chern SR; Wu PS; Chen YN; Chen SW; Yang CW; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2016 Dec; 55(6):856-860. PubMed ID: 28040133
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 18 at amniocentesis in a pregnancy with a favorable fetal outcome and maternal uniparental disomy 18.
Chen CP; Su JW; Chern SR; Wu PS; Chen SW; Wu FT; Chen WL; Lee MS; Pan CW; Chen YY; Wang W
Taiwan J Obstet Gynecol; 2022 Jul; 61(4):684-689. PubMed ID: 35779922
[TBL] [Abstract][Full Text] [Related]
38. Low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a positive NIPT result suspicious of trisomy 13, a CVS result of mosaic trisomy 13, cytogenetic discrepancy in various tissues and a favorable fetal outcome.
Chen CP; Chen M; Ma GC; Chang SP; Wu FT; Pan YT; Chern SR; Chen WL; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2023 Jul; 62(4):577-581. PubMed ID: 37407198
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome.
Chen CP; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2017 Dec; 56(6):840-842. PubMed ID: 29241931
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
