91 related articles for article (PubMed ID: 24298912)
1. Transabdominal coelocentesis as early source of fetal DNA for chromosomal and molecular diagnosis.
Pietropolli A; Vicario R; Peconi C; Zampatti S; Quitadamo MC; Capogna MV; Ragazzo M; Nardone AM; Postorivo D; Spitalieri P; Sarta S; Ratto F; Novelli G; Sangiuolo F; Piccione E; Giardina E
J Matern Fetal Neonatal Med; 2014 Nov; 27(16):1656-60. PubMed ID: 24298912
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis using combined quantitative fluorescent polymerase chain reaction and array comparative genomic hybridization analysis as a first-line test: results from over 1000 consecutive cases.
Scott F; Murphy K; Carey L; Greville W; Mansfield N; Barahona P; Robertson R; McLennan A
Ultrasound Obstet Gynecol; 2013 May; 41(5):500-7. PubMed ID: 23401365
[TBL] [Abstract][Full Text] [Related]
3. Very early prenatal diagnosis of Cockayne's syndrome by coelocentesis.
Giambona A; Vinciguerra M; Leto F; Cassarà F; Cucinella G; Cigna V; Orlandi E; Piccione M; Picciotto F; Maggio A
J Obstet Gynaecol; 2022 Jul; 42(5):1524-1531. PubMed ID: 35006018
[TBL] [Abstract][Full Text] [Related]
4. The detection of aneuploidy and maternal contamination by QF-PCR in samples undergoing prenatal diagnosis for thalassemia in Southern China.
Liao C; Yang X; Li FT; Li J; Li DZ
Eur J Obstet Gynecol Reprod Biol; 2009 Jun; 144(2):149-52. PubMed ID: 19375212
[TBL] [Abstract][Full Text] [Related]
5. Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases.
Fiorentino F; Caiazzo F; Napolitano S; Spizzichino L; Bono S; Sessa M; Nuccitelli A; Biricik A; Gordon A; Rizzo G; Baldi M
Prenat Diagn; 2011 Dec; 31(13):1270-82. PubMed ID: 22034057
[TBL] [Abstract][Full Text] [Related]
6. Very early prenatal diagnosis of genetic diseases based on coelomic fluid analysis: a feasibility study.
Jouannic JM; Costa JM; Ernault P; Bénifla JL
Hum Reprod; 2006 Aug; 21(8):2185-8. PubMed ID: 16769753
[TBL] [Abstract][Full Text] [Related]
7. Coelocentesis: a new technique for early prenatal diagnosis.
Jurkovic D; Jauniaux E; Campbell S; Pandya P; Cardy DL; Nicolaides KH
Lancet; 1993 Jun; 341(8861):1623-4. PubMed ID: 8099993
[TBL] [Abstract][Full Text] [Related]
8. [Application of multiplex quantitative fluorescent PCR with non-polymorphic loci in prenatal diagnosis].
Zhu XY; Hu YL; Wang YP; Zhu HY; Li J; Zhu RF; Zhang Y; Wu X; Yang Y
Zhonghua Fu Chan Ke Za Zhi; 2008 Nov; 43(11):818-23. PubMed ID: 19087563
[TBL] [Abstract][Full Text] [Related]
9. Early prenatal diagnosis: standard cytogenetic analysis of coelomic cells obtained by coelocentesis.
Crüger DG; Bruun-Petersen G; Kølvraa S
Prenat Diagn; 1996 Oct; 16(10):945-9. PubMed ID: 8938067
[TBL] [Abstract][Full Text] [Related]
10. Aneuploidy screening in coelomic samples using fluorescence in situ hybridisation (FISH).
Chatzimeletiou K; Makrydimas G; Sotiriadis A; Paraskevaidis E; Nicolaides KH
Prenat Diagn; 2005 Oct; 25(10):919-26. PubMed ID: 16103986
[TBL] [Abstract][Full Text] [Related]
11. The introduction of QF-PCR in prenatal diagnosis of fetal aneuploidies: time for reconsideration.
Nicolini U; Lalatta F; Natacci F; Curcio C; Bui TH
Hum Reprod Update; 2004; 10(6):541-8. PubMed ID: 15514017
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis using array-CGH: a French experience.
Rooryck C; Toutain J; Cailley D; Bouron J; Horovitz J; Lacombe D; Arveiler B; Saura R
Eur J Med Genet; 2013 Jul; 56(7):341-5. PubMed ID: 23454632
[TBL] [Abstract][Full Text] [Related]
13. Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH.
Bi W; Breman AM; Venable SF; Eng PA; Sahoo T; Lu XY; Patel A; Beaudet AL; Cheung SW; White LD
Prenat Diagn; 2008 Oct; 28(10):943-9. PubMed ID: 18792925
[TBL] [Abstract][Full Text] [Related]
14. Maternal cell contamination of prenatal samples assessed by QF-PCR genotyping.
Stojilkovic-Mikic T; Mann K; Docherty Z; Mackie Ogilvie C
Prenat Diagn; 2005 Jan; 25(1):79-83. PubMed ID: 15662689
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of chromosomal mosaicism in over 1600 cases using array comparative genomic hybridization as a first line test.
Carey L; Scott F; Murphy K; Mansfield N; Barahona P; Leigh D; Robertson R; McLennan A
Prenat Diagn; 2014 May; 34(5):478-86. PubMed ID: 24453008
[TBL] [Abstract][Full Text] [Related]
16. Prenatal paternity testing using DNA extracted from coelomic cells.
Makrydimas G; Georgiou I; Kranas V; Kaponis A; Lolis D
Fetal Diagn Ther; 2004; 19(1):75-7. PubMed ID: 14646423
[TBL] [Abstract][Full Text] [Related]
17. Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies.
Lee CN; Lin SY; Lin CH; Shih JC; Lin TH; Su YN
BJOG; 2012 Apr; 119(5):614-25. PubMed ID: 22313859
[TBL] [Abstract][Full Text] [Related]
18. [Advances in rapid prenatal detection of fetal chromosome abnormalities].
Wang J; Cui YX
Zhonghua Nan Ke Xue; 2010 Apr; 16(4):359-63. PubMed ID: 20626168
[TBL] [Abstract][Full Text] [Related]
19. Fetal nuchal translucency scan and early prenatal diagnosis of chromosomal abnormalities by rapid aneuploidy screening: observational study.
Chitty LS; Kagan KO; Molina FS; Waters JJ; Nicolaides KH
BMJ; 2006 Feb; 332(7539):452-5. PubMed ID: 16476673
[TBL] [Abstract][Full Text] [Related]
20. QF-PCR rapid aneuploidy screen and aCGH analysis of cell free fetal (cff) DNA in supernatant of compromised amniotic fluids (AF).
Madjunkova S; Tong Li C; Vlasschaert M; Adams M; Chitayat D; Maire G; Kolomietz E
Prenat Diagn; 2014 Oct; 34(10):970-6. PubMed ID: 24801814
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
