437 related articles for article (PubMed ID: 22212321)
1. Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb.
Chen CP; Chern SR; Chen CY; Wu PC; Chen LF; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):479-84. PubMed ID: 22212321
[TBL] [Abstract][Full Text] [Related]
2. Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
Chen CP; Chern SR; Lee CC; Chang TY; Wang W; Tzen CY
Prenat Diagn; 2004 Jan; 24(1):38-44. PubMed ID: 14755408
[TBL] [Abstract][Full Text] [Related]
3. Alobar holoprosencephaly, cebocephaly, and micropenis in a Klinefelter fetus of a diabetic mother.
Chen CP; Su TH; Chern SR; Su JW; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2012 Dec; 51(4):630-4. PubMed ID: 23276570
[TBL] [Abstract][Full Text] [Related]
4. Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
Chen CP; Su YN; Chen YY; Su JW; Chern SR; Chen YT; Chen WL; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):506-11. PubMed ID: 22212326
[TBL] [Abstract][Full Text] [Related]
5. Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses.
Chen CP; Lin HM; Su YN; Chern SR; Tsai FJ; Wu PC; Lee CC; Chen YT; Lee MS; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2010 Sep; 49(3):341-50. PubMed ID: 21056321
[TBL] [Abstract][Full Text] [Related]
6. Rapid diagnosis of trisomy 18 of maternal origin by quantitative fluorescent polymerase chain reaction analysis following tissue culture failure for conventional cytogenetic analysis in a fetus with holoprosencephaly, ventricular septal defect, arthrogryposis of bilateral wrists and aplasia of the thumbs.
Chen CP; Weng SS; Chern SR; Chen SW; Wu FT; Wang W
Taiwan J Obstet Gynecol; 2021 May; 60(3):549-550. PubMed ID: 33966746
[TBL] [Abstract][Full Text] [Related]
7. [Edwards syndrome--most frequent indications for genetic amniocentesis. Analysis of the last 5 years].
Chuchracki M; Janiak J; Ziółkowska K; Sedziak A; Opala T
Przegl Lek; 2012; 69(10):1007-10. PubMed ID: 23421080
[TBL] [Abstract][Full Text] [Related]
8. Monozygotic twins with trisomy 18 of paternal origin: prenatal diagnosis and molecular cytogenetic characterization in a pregnancy with one structurally abnormal living fetus and one intrauterine fetal demise.
Chen CP; Chern SR; Chen YY; Wu PC; Town DD; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2012 Sep; 51(3):430-4. PubMed ID: 23040931
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
[TBL] [Abstract][Full Text] [Related]
10. Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism.
Biselli JM; Machado FB; Zampieri BL; Alves da Silva AF; Goloni-Bertollo EM; Haddad R; Eberlin MN; Vannucchi H; Carvalho VM; Medina-Acosta E; Pavarino-Bertelli EC
Genet Couns; 2009; 20(3):225-34. PubMed ID: 19852428
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Wu PC; Chen WL; Chen LF; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2011 Jun; 50(2):188-95. PubMed ID: 21791306
[TBL] [Abstract][Full Text] [Related]
14. Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction.
Chen CP; Su YN; Chen YY; Chern SR; Liu YP; Wu PC; Lee CC; Chen YT; Wang W
Taiwan J Obstet Gynecol; 2011 Sep; 50(3):345-52. PubMed ID: 22030051
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Prenatal diagnosis of a fetus with partial trisomy 7p.
Ozgun MT; Batukan C; Basbug M; Akgun H; Caglayan O; Dundar M
Fetal Diagn Ther; 2007; 22(3):229-32. PubMed ID: 17228165
[TBL] [Abstract][Full Text] [Related]
17. Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
Chen CP; Chen M; Su YN; Hsu CY; Tsai FJ; Chern SR; Wu PC; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2010 Dec; 49(4):473-80. PubMed ID: 21199750
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
[TBL] [Abstract][Full Text] [Related]
19. A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
Chen CP; Huang HK; Ling PY; Su YN; Chen M; Tsai FJ; Wu PC; Chern SR; Chen YT; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):492-8. PubMed ID: 22212323
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of multiple pterygium syndrome associated with Klinefelter syndrome.
Lembet A; Oktem M; Yilmaz Z; Kaya U; Derbent M
Prenat Diagn; 2003 Sep; 23(9):728-30. PubMed ID: 12975782
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
