583 related articles for article (PubMed ID: 21199755)
21. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.
Chen CP; Lin SP; Lin YH; Chern SR; Wu PS; Chen YN; Chen SW; Yang CW; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2016 Dec; 55(6):852-855. PubMed ID: 28040132
[TBL] [Abstract][Full Text] [Related]
22. Pure partial monosomy 3p (3p25.3 → pter): prenatal diagnosis and array comparative genomic hybridization characterization.
Chen CP; Su YN; Chen CY; Su JW; Chern SR; Town DD; Wang W
Taiwan J Obstet Gynecol; 2012 Sep; 51(3):435-9. PubMed ID: 23040932
[TBL] [Abstract][Full Text] [Related]
23. Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion.
Chen CP; Chen CY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Lee MS; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Oct; 55(5):705-711. PubMed ID: 27751420
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
[TBL] [Abstract][Full Text] [Related]
26. Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.
Chen CP; Lin SP; Chern SR; Shih SL; Lee CC; Wang W; Liao YW
Prenat Diagn; 2003 Jun; 23(6):504-8. PubMed ID: 12813767
[TBL] [Abstract][Full Text] [Related]
27. Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication.
Chen CP; Huang JP; Chern SR; Wu PS; Chen SW; Wu FT; Chen WL; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2020 Jan; 59(1):140-145. PubMed ID: 32039783
[TBL] [Abstract][Full Text] [Related]
28. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis.
Chen CP; Chen CY; Chern SR; Wu PS; Chen SW; Lee CC; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2020 Jan; 59(1):130-134. PubMed ID: 32039781
[TBL] [Abstract][Full Text] [Related]
29. Prenatal detection of a subtle unbalanced chromosome rearrangement by karyotyping, FISH and array comparative genomic hybridization.
Cain CC; Saul DO; Oehler E; Blakemore K; Stetten G
Fetal Diagn Ther; 2008; 24(3):286-90. PubMed ID: 18818501
[TBL] [Abstract][Full Text] [Related]
30. Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 1q42.3-q44 deletion in a fetus associated with ventriculomegaly on prenatal ultrasound.
Chen CP; Ko TM; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2020 Jul; 59(4):598-603. PubMed ID: 32653137
[TBL] [Abstract][Full Text] [Related]
31. Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly.
Chen CP; Kuo YK; Su YN; Chern SR; Tsai FJ; Wu PC; Chen YT; Town DD; Wang W
Taiwan J Obstet Gynecol; 2011 Jun; 50(2):182-7. PubMed ID: 21791305
[TBL] [Abstract][Full Text] [Related]
32. Partial trisomy 2q(2q37.3-->qter) and monosomy 7q(7q34--->qter) due to paternal reciprocal translocation 2;7: a case report.
Ahn JM; Koo DH; Kwon KW; Lee YK; Lee YH; Lee HH; Nam KH; Lee KH
J Korean Med Sci; 2003 Feb; 18(1):112-3. PubMed ID: 12589098
[TBL] [Abstract][Full Text] [Related]
33. Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
Chen CP; Su YN; Hsu CY; Chern SR; Lee CC; Chen YT; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):485-91. PubMed ID: 22212322
[TBL] [Abstract][Full Text] [Related]
34. Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1-q21.2 and 5-Mb deletion of 21q22.3.
Chen CP; Lin YH; Chou SY; Su YN; Chern SR; Chen YT; Town DD; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2012 Mar; 51(1):71-6. PubMed ID: 22482972
[TBL] [Abstract][Full Text] [Related]
35. De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1 → pter) and 14q (14q32.31 → qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction, and single umbilical artery: prenatal diagnosis and molecular cytogenetic characterization.
Chen CP; Fu CH; Chern SR; Wu PS; Su JW; Lee CC; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2013 Sep; 52(3):401-6. PubMed ID: 24075381
[TBL] [Abstract][Full Text] [Related]
36. Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3:1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2).
Chen CP; Chern SR; Lee CC; Town DD; Chen WL; Wang W
Prenat Diagn; 1999 Aug; 19(8):783-6. PubMed ID: 10451531
[TBL] [Abstract][Full Text] [Related]
37. Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum.
Chen CP; Hsu CY; Chern SR; Wu PS; Chen SW; Wang W
Taiwan J Obstet Gynecol; 2020 Jan; 59(1):127-129. PubMed ID: 32039780
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
Chen CP; Devriendt K; Lee CC; Chen WL; Wang W; Wang TY
Prenat Diagn; 1999 Oct; 19(10):986-9. PubMed ID: 10521829
[TBL] [Abstract][Full Text] [Related]
40. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.
Chen CP; Ko TM; Su YN; Wang LK; Chern SR; Wu PS; Chen YN; Chen SW; Ko K; Lee CC; Chen LF; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Oct; 55(5):733-737. PubMed ID: 27751426
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]