184 related articles for article (PubMed ID: 24824252)
1. Prenatal diagnosis of Down syndrome using cell-free fetal DNA in amniotic fluid by quantitative fluorescent polymersase chain reaction.
Wu D; Chi H; Shao M; Wu Y; Jin H; Wu B; Qiao J
Chin Med J (Engl); 2014; 127(10):1897-901. PubMed ID: 24824252
[TBL] [Abstract][Full Text] [Related]
2. Human chromosome 21-specific DNA markers are useful in prenatal detection of Down syndrome.
Liou JD; Chu DC; Cheng PJ; Chang SD; Sun CF; Wu YC; Liou WY; Chiu DT
Ann Clin Lab Sci; 2004; 34(3):319-23. PubMed ID: 15487707
[TBL] [Abstract][Full Text] [Related]
3. [Rapid detection of the most common chromosomal aneuploidies in the second-trimester amniotic fluid using QF-PCR].
Švecová I; Burjanivová T; Kršiaková J; Lasabová Z; Biringer K; Kapustová I; Móricová P; Danko J
Ceska Gynekol; 2013 Aug; 78(4):373-8. PubMed ID: 24040987
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of common aneuploidies using multiplex quantitative fluorescent polymerase chain reaction.
El Mouatassim S; Becker M; Kuzio S; Ronsin C; Gil S; Nouchy M; Druard L; Forestier F
Fetal Diagn Ther; 2004; 19(6):496-503. PubMed ID: 15539874
[TBL] [Abstract][Full Text] [Related]
5. Rapid prenatal diagnosis of Down Syndrome using quantitative fluorescent PCR in uncultured amniocytes.
Lee MH; Ryu HM; Kim DJ; Lee BY; Cho EH; Yang JH; Kim MY; Han JY; Park SY
J Korean Med Sci; 2004 Jun; 19(3):341-4. PubMed ID: 15201497
[TBL] [Abstract][Full Text] [Related]
6. [Use of quantitative fluorescence polymerase chain reaction in the invasive prenatal diagnosis of Down's syndrome].
Kriventsova NV; Shokarev RA; Avrutskaia VV; Kriger SIu; Klochkova NE; Gimbut VS; Kornienko IV
Klin Lab Diagn; 2010 Aug; (8):27-30. PubMed ID: 20891040
[TBL] [Abstract][Full Text] [Related]
7. Rapid prenatal diagnosis of aneuploidy for chromosomes 21, 18, 13, and X by quantitative fluorescence polymerase chain reaction.
Ochshorn Y; Bar-Shira A; Jonish A; Yaron Y
Fetal Diagn Ther; 2006; 21(4):326-31. PubMed ID: 16757905
[TBL] [Abstract][Full Text] [Related]
8. [Detection of trisomy 21 by quantitative fluorescent PCR in clinical samples undergoing prenatal diagnosis for hereditary hearing loss].
Lu YP; Cheng J; Han B; Wang LX; Dai P; Yuan HJ; Li YL
Zhonghua Fu Chan Ke Za Zhi; 2011 Jun; 46(6):427-30. PubMed ID: 21781583
[TBL] [Abstract][Full Text] [Related]
9. [Practicality of rapid prenatal screening for Down syndrome with PCR-short tandem repeat method].
Guan L; Ren C; Li H; Gao L; Jia N; Guan H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Jun; 30(3):277-82. PubMed ID: 23744314
[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. Quantitative real-time PCR technique for rapid prenatal diagnosis of Down syndrome.
Hu Y; Zheng M; Xu Z; Wang X; Cui H
Prenat Diagn; 2004 Sep; 24(9):704-7. PubMed ID: 15386450
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. Determination of sensitivity and specificity of a novel gene dosage assay for prenatal screening of trisomy 21 syndrome.
Kamyab AR; Shahrokhi F; Shamsian E; Hayat Nosaied M; Dibajnia P; Hashemi M; Mahdian R
Clin Biochem; 2012 Feb; 45(3):267-71. PubMed ID: 22178108
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of trisomy 21 by quantitatively pyrosequencing heterozygotes using amniotic fluid as starting material of PCR.
Ye H; Wu H; Huang H; Liu Y; Zou B; Sun L; Zhou G
Analyst; 2013 Apr; 138(8):2443-8. PubMed ID: 23463136
[TBL] [Abstract][Full Text] [Related]
15. Rapid prenatal diagnosis of trisomy 21 by real-time quantitative polymerase chain reaction with amplification of small tandem repeats and S100B in chromosome 21.
Yang YH; Nam MS; Yang ES
Yonsei Med J; 2005 Apr; 46(2):193-7. PubMed ID: 15861490
[TBL] [Abstract][Full Text] [Related]
16. Detection of parental origin and cell stage errors of a double nondisjunction in a fetus by QF-PCR.
Guzel AI; Demirhan O; Pazarbasi A; Ozgunen FT; Kocaturk-Sel S; Tastemir D
Genet Test Mol Biomarkers; 2009 Feb; 13(1):73-7. PubMed ID: 19309277
[TBL] [Abstract][Full Text] [Related]
17. [Diagnosis of Down's syndrome using short tandem repeat loci D21S11, D21S1440 and Penta D].
Shi YF; Li XZ; Li Y; Zhang XL; Zhang Y; Yue TF
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):443-6. PubMed ID: 22875503
[TBL] [Abstract][Full Text] [Related]
18. [Prenatal diagnosis of fetal chromosomal aneuploidies using quantitative fluorescent PCR (QF-PCR)].
Nakonieczny M; Jezierski G; Woźniak I; Liss J; Pawłowski R; Preis K; Swiatkowska-Freund M; Wójcikowski C; Łukaszuk K
Przegl Lek; 2008; 65(3):119-21. PubMed ID: 18624118
[TBL] [Abstract][Full Text] [Related]
19. Detection of trisomy 21 by quantitative fluorescent-polymerase chain reaction in uncultured amniocytes.
Solassol J; Rahil H; Sapin V; Lemery D; Dastugue B; Boespflug-Tanguy O; Creveaux I
Prenat Diagn; 2003 Apr; 23(4):287-91. PubMed ID: 12673631
[TBL] [Abstract][Full Text] [Related]
20. Rapid prenatal diagnosis of common aneuploidies in amniotic fluid using quantitative fluorescent polymerase chain reaction.
Onay H; Ugurlu T; Aykut A; Pehlivan S; Inal M; Tinar S; Ozkinay C; Ozkinay F
Gynecol Obstet Invest; 2008; 66(2):104-10. PubMed ID: 18446039
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
