163 related articles for article (PubMed ID: 25951728)
1. First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism.
Chen CP; Wang LK; Chern SR; Kuo YL; Chen YN; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2015 Apr; 54(2):194-5. PubMed ID: 25951728
[No Abstract] [Full Text] [Related]
2. Concomitant omphalocele, anencephaly and arthrogryposis associated with trisomy 18.
Karaman A; Aydin H; Göksu K
Genet Couns; 2015; 26(1):77-9. PubMed ID: 26043511
[No Abstract] [Full Text] [Related]
3. Prenatally diagnosed mosaic trisomy 14q with omphalocele.
Wang JC; Li CF; Shaw DR
Prenat Diagn; 2007 Dec; 27(13):1260-1. PubMed ID: 17994633
[No Abstract] [Full Text] [Related]
4. Concomitant omphalocele and anencephaly associated with trisomy 18 and arthrogryposis diagnosed in early pregnancy.
Chen CP; Chang TY; Lin HH; Chern SR; Wang W
Taiwan J Obstet Gynecol; 2008 Mar; 47(1):93-4. PubMed ID: 18400591
[No Abstract] [Full Text] [Related]
5. Ruptured omphalocele mimicking gastroschisis in a fetus with Edwards syndrome.
Betat Rda S; Telles JA; Gobatto AM; Bicca AM; Arcolini CP; Dal Pai TK; Faria AE; Zen PR; Rosa RF
Am J Med Genet A; 2014 Feb; 164A(2):559-60. PubMed ID: 24132880
[No Abstract] [Full Text] [Related]
6. Rapid detection of maternal origin of trisomy 18 by quantitative fluorescent polymerase chain reaction in a fetus associated with increased nuchal translucency thickness and omphalocele on first-trimester prenatal ultrasound.
Chen CP
Taiwan J Obstet Gynecol; 2024 Mar; 63(2):272-275. PubMed ID: 38485332
[No Abstract] [Full Text] [Related]
7. Misdiagnosis of omphalocele associated with Edwards syndrome and congenital heart disease.
Colley N; Knott PD; Gould SJ
Prenat Diagn; 1987 Jun; 7(5):377-81. PubMed ID: 3303007
[TBL] [Abstract][Full Text] [Related]
8. First-trimester tests for trisomies 21 and 18 as sensitive as triple screen.
Lewis PR; Pasalio R
J Fam Pract; 2004 Mar; 53(3):184-6. PubMed ID: 15000919
[No Abstract] [Full Text] [Related]
9. Confined placental origin of the circulating cell free fetal DNA revealed by a discordant non-invasive prenatal test result in a trisomy 18 pregnancy.
Mao J; Wang T; Wang BJ; Liu YH; Li H; Zhang J; Cram D; Chen Y
Clin Chim Acta; 2014 Jun; 433():190-3. PubMed ID: 24667696
[TBL] [Abstract][Full Text] [Related]
10. Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysis.
Donaghue C; Mann K; Docherty Z; Ogilvie CM
Prenat Diagn; 2005 Jan; 25(1):65-72. PubMed ID: 15662691
[TBL] [Abstract][Full Text] [Related]
11. Non-invasive prenatal testing of trisomy 18 by an epigenetic marker in first trimester maternal plasma.
Lee DE; Kim SY; Lim JH; Park SY; Ryu HM
PLoS One; 2013; 8(11):e78136. PubMed ID: 24223769
[TBL] [Abstract][Full Text] [Related]
12. Screening for trisomies by cell-free DNA testing of maternal blood: consequences of a failed result.
Revello R; Sarno L; Ispas A; Akolekar R; Nicolaides KH
Ultrasound Obstet Gynecol; 2016 Jun; 47(6):698-704. PubMed ID: 26743020
[TBL] [Abstract][Full Text] [Related]
13. [Combined first trimester screening and cell-free fetal DNA - “next generation screening”].
Kagan KO; Eiben B; Kozlowski P
Ultraschall Med; 2014 Jun; 35(3):229-36. PubMed ID: 24764214
[TBL] [Abstract][Full Text] [Related]
14. Birth prevalence and survival of exomphalos in england and wales: 2005 to 2011.
Springett A; Draper ES; Rankin J; Rounding C; Tucker D; Stoianova S; Wellesley D; Morris JK
Birth Defects Res A Clin Mol Teratol; 2014 Sep; 100(9):721-5. PubMed ID: 25178262
[TBL] [Abstract][Full Text] [Related]
15. Rapid diagnosis of maternal origin of fetal trisomy 13 by quantitative fluorescent polymerase chain reaction in a pregnancy associated with young maternal age and omphalocele on prenatal ultrasound.
Chen CP
Taiwan J Obstet Gynecol; 2024 Jan; 63(1):108-110. PubMed ID: 38216245
[No Abstract] [Full Text] [Related]
16. Neural tube defects and omphalocele in trisomy 18.
van Maldergem L; Gillerot Y; Koulischer L
Clin Genet; 1989 Jan; 35(1):77-8. PubMed ID: 2924433
[No Abstract] [Full Text] [Related]
17. Prenatal diagnosis of trisomy 6 mosaicism.
Destree A; Fourneau C; Dugauquier C; Rombout S; Sartenaer D; Gillerot Y
Prenat Diagn; 2005 May; 25(5):354-7. PubMed ID: 15906424
[TBL] [Abstract][Full Text] [Related]
18. Trisomy 16 detected by first trimester screening.
Petracchi F; Igarzabal L; Crespo ML; Gadow E
Prenat Diagn; 2009 Dec; 29(12):1175-6. PubMed ID: 19777531
[No Abstract] [Full Text] [Related]
19. Improvement of a prenatal screening program for trisomy 18 in the first trimester of gestation.
Martínez-Morillo E; Prieto B; Moreno F; Alvarez FV
Clin Chem Lab Med; 2012 Nov; 50(11):1973-7. PubMed ID: 23092801
[TBL] [Abstract][Full Text] [Related]
20. Increased risk after noninvasive prenatal screening on cell-free DNA circulating in maternal blood: does a new indication for invasive prenatal diagnosis require new criteria for confirmatory cytogenetic analysis?
Grati FR; Malvestiti F; Grimi B; Liuti R; Agrati C; Gaetani E; Milani S; Martinoni L; Zanatta V; Gallazzi G; Maggi F; Simoni G
Prenat Diagn; 2015 Mar; 35(3):308-9. PubMed ID: 25754154
[No Abstract] [Full Text] [Related]
[Next] [New Search]
