206 related articles for article (PubMed ID: 22506923)
1. Fetal DNA in maternal plasma: a noninvasive tool for prenatal diagnosis of beta-thalassemia.
Galbiati S; Brisci A; Damin F; Gentilin B; Curcio C; Restagno G; Cremonesi L; Ferrari M
Expert Opin Biol Ther; 2012 Jun; 12 Suppl 1():S181-7. PubMed ID: 22506923
[TBL] [Abstract][Full Text] [Related]
2. Application of maternal plasma DNA analysis for noninvasive prenatal diagnosis of Hb E-beta-thalassemia.
Tungwiwat W; Fucharoen G; Fucharoen S; Ratanasiri T; Sanchaisuriya K; Sae-Ung N
Transl Res; 2007 Nov; 150(5):319-25. PubMed ID: 17964521
[TBL] [Abstract][Full Text] [Related]
3. Multiplex fluorescent PCR for noninvasive prenatal detection of fetal-derived paternally inherited diseases using circulatory fetal DNA in maternal plasma.
Tang DL; Li Y; Zhou X; Li X; Zheng F
Eur J Obstet Gynecol Reprod Biol; 2009 May; 144(1):35-9. PubMed ID: 19285775
[TBL] [Abstract][Full Text] [Related]
4. Size fractionation of cell-free DNA in maternal plasma and its application in noninvasive detection of fetal single gene point mutations.
Li Y; Holzgreve W; Hahn S
Methods Mol Biol; 2008; 444():239-51. PubMed ID: 18425486
[TBL] [Abstract][Full Text] [Related]
5. [Prenatal diagnosis of β-thalassaemia using cell-free fetal DNA in maternal plasma].
Li GH; Rong KB; Luo YF; Chen D; Gong CP; Wu J; DI YW; Ge YF
Nan Fang Yi Ke Da Xue Xue Bao; 2011 Aug; 31(8):1437-9. PubMed ID: 21868341
[TBL] [Abstract][Full Text] [Related]
6. Detection of paternally inherited fetal point mutations for β-thalassemia in maternal plasma using simple fetal DNA enrichment protocol with or without whole genome amplification: an accuracy assessment.
Ramezanzadeh M; Salehi M; Farajzadegan Z; Kamali S; Salehi R
J Matern Fetal Neonatal Med; 2016; 29(16):2645-9. PubMed ID: 26553322
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of beta-thalassemia in Egypt: implementing accurate high-tech methods did not reflect much on the outcome.
Elgawhary S; Elbaradie Sahar MY; Rashad WM; Mosaad M; Abdalla MA; Ezzat G; Wali YA; Elbeshlawy A
Pediatr Hematol Oncol; 2008 Sep; 25(6):541-8. PubMed ID: 18728973
[TBL] [Abstract][Full Text] [Related]
8. Feasibility study of using fetal DNA in maternal plasma for non-invasive prenatal diagnosis.
Liu FM; Wang XY; Feng X; Wang W; Ye YX; Chen H
Acta Obstet Gynecol Scand; 2007; 86(5):535-41. PubMed ID: 17464580
[TBL] [Abstract][Full Text] [Related]
9. COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasma.
Galbiati S; Monguzzi A; Damin F; Soriani N; Passiu M; Castellani C; Natacci F; Curcio C; Seia M; Lalatta F; Chiari M; Ferrari M; Cremonesi L
J Med Genet; 2016 Jul; 53(7):481-7. PubMed ID: 26912453
[TBL] [Abstract][Full Text] [Related]
10. Recent advances in fetal nucleic acids in maternal plasma.
Lo YM
J Histochem Cytochem; 2005 Mar; 53(3):293-6. PubMed ID: 15750005
[TBL] [Abstract][Full Text] [Related]
11. Application of fetal DNA in maternal plasma for noninvasive prenatal diagnosis.
Chiu RW; Lo YM
Expert Rev Mol Diagn; 2002 Jan; 2(1):32-40. PubMed ID: 11963800
[TBL] [Abstract][Full Text] [Related]
12. Non-invasive prenatal diagnosis of β-thalassemia by detection of the cell-free fetal DNA in maternal circulation: a systematic review and meta-analysis.
Zafari M; Kosaryan M; Gill P; Alipour A; Shiran M; Jalalli H; Banihashemi A; Fatahi F
Ann Hematol; 2016 Aug; 95(8):1341-50. PubMed ID: 26968552
[TBL] [Abstract][Full Text] [Related]
13. Prenatal detection of beta-thalassemia CD17 (A-->T) mutation by polymerase chain reaction/ligase detection reaction/capillary electrophoresis for fetal DNA in maternal plasma--a case report.
Yi P; Chen Z; Yu L; Zheng Y; Xie H; Zheng X; Liu Q; Han J; Li L
Fetal Diagn Ther; 2010; 27(1):25-31. PubMed ID: 19955703
[TBL] [Abstract][Full Text] [Related]
14. Noninvasive prenatal diagnosis experience in the Çukurova Region of Southern Turkey: detecting paternal mutations of sickle cell anemia and β-thalassemia in cell-free fetal DNA using high-resolution melting analysis.
Yenilmez ED; Tuli A; Evrüke IC
Prenat Diagn; 2013 Nov; 33(11):1054-62. PubMed ID: 23836351
[TBL] [Abstract][Full Text] [Related]
15. Size fractionation of cell-free DNA in maternal plasma improves the detection of a paternally inherited beta-thalassemia point mutation by MALDI-TOF mass spectrometry.
Li Y; Di Naro E; Vitucci A; Grill S; Zhong XY; Holzgreve W; Hahn S
Fetal Diagn Ther; 2009; 25(2):246-9. PubMed ID: 19506384
[TBL] [Abstract][Full Text] [Related]
16. [Prenatal gene diagnosis of paternally inherited alpha-thalassemia by detecting fetal DNA in maternal plasma].
Chen P; Li MJ; Li MQ; Li SQ; Zhou LY; Lin WX
Zhonghua Yi Xue Za Zhi; 2007 Jun; 87(22):1540-4. PubMed ID: 17785106
[TBL] [Abstract][Full Text] [Related]
17. Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma.
Li Y; Di Naro E; Vitucci A; Zimmermann B; Holzgreve W; Hahn S
JAMA; 2005 Feb; 293(7):843-9. PubMed ID: 15713774
[TBL] [Abstract][Full Text] [Related]
18. Fast Temperature-Gradient COLD PCR for the enrichment of the paternally inherited SNPs in cell free fetal DNA; an application to non-invasive prenatal diagnosis of β-thalassaemia.
Byrou S; Makrigiorgos GM; Christofides A; Kallikas I; Papasavva T; Kleanthous M
PLoS One; 2018; 13(7):e0200348. PubMed ID: 30044883
[TBL] [Abstract][Full Text] [Related]
19. Non-invasive prenatal diagnosis by fetal nucleic acid analysis in maternal plasma: the coming of age.
Chiu RW; Lo YM
Semin Fetal Neonatal Med; 2011 Apr; 16(2):88-93. PubMed ID: 21075065
[TBL] [Abstract][Full Text] [Related]
20. [Improvement of detection of paternally inherited fetal mutant genes for β-globin in maternal plasma by PNA clamp].
Huang K; Pan HF
Zhonghua Xue Ye Xue Za Zhi; 2013 Mar; 34(3):233-6. PubMed ID: 23683423
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
