213 related articles for article (PubMed ID: 25200820)
1. Association of non-invasive prenatal testing and chromosomal microarray analysis for prenatal diagnostics.
Korostelev S; Totchiev G; Kanivets I; Gnetetskaya V
Gynecol Endocrinol; 2014 Oct; 30 Suppl 1():13-6. PubMed ID: 25200820
[TBL] [Abstract][Full Text] [Related]
2. The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies.
Srebniak MI; Knapen MFCM; Polak M; Joosten M; Diderich KEM; Govaerts LCP; Boter M; Kromosoeto JNR; van Hassel DACM; Huijbregts G; van IJcken WFJ; Heydanus R; Dijkman A; Toolenaar T; de Vries FAT; Knijnenburg J; Go ATJI; Galjaard RH; Van Opstal D
Hum Mutat; 2017 Jul; 38(7):880-888. PubMed ID: 28409863
[TBL] [Abstract][Full Text] [Related]
3. Aneuploidy screening by non-invasive prenatal testing in twin pregnancy.
Fosler L; Winters P; Jones KW; Curnow KJ; Sehnert AJ; Bhatt S; Platt LD
Ultrasound Obstet Gynecol; 2017 Apr; 49(4):470-477. PubMed ID: 27194226
[TBL] [Abstract][Full Text] [Related]
4. Secondary findings from non-invasive prenatal testing for common fetal aneuploidies by whole genome sequencing as a clinical service.
Lau TK; Jiang FM; Stevenson RJ; Lo TK; Chan LW; Chan MK; Lo PS; Wang W; Zhang HY; Chen F; Choy KW
Prenat Diagn; 2013 Jun; 33(6):602-8. PubMed ID: 23553438
[TBL] [Abstract][Full Text] [Related]
5. Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y.
Nicolaides KH; Syngelaki A; Gil M; Atanasova V; Markova D
Prenat Diagn; 2013 Jun; 33(6):575-9. PubMed ID: 23613152
[TBL] [Abstract][Full Text] [Related]
6. [Clinical application of noninvasive prenatal diagnosis using cell free fetal DNA in maternal plasma].
Hou QF; Wu D; Chu Y; Kang B; Liao SX; Yang YL; Zhang CY; Zhang JX; Wu G
Zhonghua Fu Chan Ke Za Zhi; 2012 Nov; 47(11):813-7. PubMed ID: 23302120
[TBL] [Abstract][Full Text] [Related]
7. Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y.
Benn P
Clin Genet; 2016 Dec; 90(6):477-485. PubMed ID: 27283893
[TBL] [Abstract][Full Text] [Related]
8. [Non-invasive prenatal test in the diagnosis of aneuploidy 13, 18 and 21--theoretical and practical aspects].
Stembalska A; Łaczmańska I; Lech D
Ginekol Pol; 2011 Feb; 82(2):126-32. PubMed ID: 21574485
[TBL] [Abstract][Full Text] [Related]
9. Detection of 21q11.2-q22.11 deletions in a fetus by NIPT.
Zheng Y; Chen B; Wan S; Xu H; Dang Y; Song T; Li Y; Zhang J
J Clin Lab Anal; 2019 Mar; 33(3):e22711. PubMed ID: 30666717
[TBL] [Abstract][Full Text] [Related]
10. Chromosomal Microarray Analysis (CMA) a Clinical Diagnostic Tool in the Prenatal and Postnatal Settings.
Batzir NA; Shohat M; Maya I
Pediatr Endocrinol Rev; 2015 Sep; 13(1):448-54. PubMed ID: 26540760
[TBL] [Abstract][Full Text] [Related]
11. The replacement of cytogenetic analysis by direct chorionic villi sampling preparation with quantitative fluorescence PCR.
Christopoulou S; Christopoulou G; Hatzaki A; Hatzipouliou A; Donoghue J; Karkaletsi M; Kaminopetros P; Sifakis S; Velissariou V
Gynecol Obstet Invest; 2009; 68(4):255-61. PubMed ID: 19776613
[TBL] [Abstract][Full Text] [Related]
12. Simultaneous identification of chromosomes 18, X and Y in uncultured amniocytes by using multi-primed in situ labelling technique.
Gadji M; Krabchi K; Drouin R
Clin Genet; 2005 Jul; 68(1):15-22. PubMed ID: 15952981
[TBL] [Abstract][Full Text] [Related]
13. Prenatal chromosomal microarray analysis and karyotyping in fetuses with isolated choroid plexus cyst: A retrospective case-control study.
Wang L; Liang P; Pan P; Su J; Qin J; Chen Z; Huang D; Sun W; Song P; Wei H
Eur J Obstet Gynecol Reprod Biol; 2024 Jun; 297():91-95. PubMed ID: 38603985
[TBL] [Abstract][Full Text] [Related]
14. Embryo morphology and development are dependent on the chromosomal complement.
Magli MC; Gianaroli L; Ferraretti AP; Lappi M; Ruberti A; Farfalli V
Fertil Steril; 2007 Mar; 87(3):534-41. PubMed ID: 17123520
[TBL] [Abstract][Full Text] [Related]
15. Preimplantation genetic screening (PGS) in infertile female age > or = 35 years by fluorescence in situ hybridization of chromosome 13, 18, 21, X and Y.
Chiamchanya C; Visutakul P; Gumnarai N; Su-angkawatin W
J Med Assoc Thai; 2008 Nov; 91(11):1644-50. PubMed ID: 19127783
[TBL] [Abstract][Full Text] [Related]
16. [Value of detection of cell-free fetal DNA in maternal plasma in the prenatal diagnosis of chromosomal abnormalities].
Wang SJ; Gao ZY; Lu YP; Li YL; You YQ; Zhang LW; Wang LX; Xu H
Zhonghua Fu Chan Ke Za Zhi; 2012 Nov; 47(11):808-12. PubMed ID: 23302119
[TBL] [Abstract][Full Text] [Related]
17. Multiplex ligation-dependent probe amplification (MLPA) in prenatal diagnosis-experience of a large series of rapid testing for aneuploidy of chromosomes 13, 18, 21, X, and Y.
Gerdes T; Kirchhoff M; Lind AM; Vestergaard Larsen G; Kjaergaard S
Prenat Diagn; 2008 Dec; 28(12):1119-25. PubMed ID: 19003800
[TBL] [Abstract][Full Text] [Related]
18. QF-PCR-based prenatal detection of aneuploidy in a southeast Asian population.
Quaife R; Wong LF; Tan SY; Chua WY; Lim SS; Hammersley CJ; Yeo HL
Prenat Diagn; 2004 Jun; 24(6):407-13. PubMed ID: 15229837
[TBL] [Abstract][Full Text] [Related]
19. Rapid prenatal diagnosis of aneuploidy using quantitative fluorescence-PCR (QF-PCR).
Ogilvie CM; Donaghue C; Fox SP; Docherty Z; Mann K
J Histochem Cytochem; 2005 Mar; 53(3):285-8. PubMed ID: 15750003
[TBL] [Abstract][Full Text] [Related]
20. Microarray-based prenatal diagnosis for the identification of fetal chromosome abnormalities.
Shaffer LG; Rosenfeld JA
Expert Rev Mol Diagn; 2013 Jul; 13(6):601-11. PubMed ID: 23895129
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
