405 related articles for article (PubMed ID: 23836351)
21. Cell-free fetal DNA in amniotic fluid supernatant for prenatal diagnosis.
Soltani M; Nemati M; Maralani M; Estiar MA; Andalib S; Fardiazar Z; Sakhinia E
Cell Mol Biol (Noisy-le-grand); 2016 Apr; 62(4):14-7. PubMed ID: 27188728
[TBL] [Abstract][Full Text] [Related]
22. Prenatal diagnosis of beta-thalassemia in the West Bank and Gaza.
Ayesh SK; Al-Sharef WA; Nassar SM; Thawabteh NA; Abu-Libdeh BY
Saudi Med J; 2005 Nov; 26(11):1771-6. PubMed ID: 16311664
[TBL] [Abstract][Full Text] [Related]
23. Rapid Detection of Fetal Mendelian Disorders: Thalassemia and Sickle Cell Syndromes.
Traeger-Synodinos J; Vrettou C; Kanavakis E
Methods Mol Biol; 2019; 1885():207-219. PubMed ID: 30506200
[TBL] [Abstract][Full Text] [Related]
24. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.
Srivorakun H; Fucharoen G; Sae-Ung N; Sanchaisuriya K; Ratanasiri T; Fucharoen S
Eur J Haematol; 2009 Jul; 83(1):57-65. PubMed ID: 19226360
[TBL] [Abstract][Full Text] [Related]
25. A fast microelectronic array for screening and prenatal diagnosis of beta-thalassemia.
Foglieni B; Galbiati S; Ferrari M; Cremonesi L
Methods Mol Biol; 2008; 444():169-82. PubMed ID: 18425480
[TBL] [Abstract][Full Text] [Related]
26. [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]
27. Prenatal molecular diagnosis of β-thalassemia and sickle cell anemia in the Syrian population.
Murad H; Moassas F; Jarjour R; Mukhalalaty Y; Al-Achkar W
Hemoglobin; 2014; 38(6):390-3. PubMed ID: 25405916
[TBL] [Abstract][Full Text] [Related]
28. Rapid detection of fetal Mendelian disorders: thalassemia and sickle cell syndromes.
Traeger-Synodinos J; Vrettou C; Kanavakis E
Methods Mol Biol; 2008; 444():133-45. PubMed ID: 18425477
[TBL] [Abstract][Full Text] [Related]
29. Prenatal diagnosis of beta-thalassemia by reverse dot-blot hybridization in southern China.
Li D; Liao C; Li J; Huang Y; Xie X; Wei J; Wu S
Hemoglobin; 2006; 30(3):365-70. PubMed ID: 16840227
[TBL] [Abstract][Full Text] [Related]
30. Prenatal diagnosis of beta-thalassemia in Southern China.
Li D; Liao C; Li J; Xie X; Huang Y; Zhong H; Wei J
Eur J Obstet Gynecol Reprod Biol; 2006; 128(1-2):81-5. PubMed ID: 16376479
[TBL] [Abstract][Full Text] [Related]
31. [Cell-free fetal DNA detection in maternal plasma using real-time PCR and cycling probe technology for prenatal screening beta-thalassaemia major].
Chen X; Ren JH; Guo H; Lin LH; Yao QX
Nan Fang Yi Ke Da Xue Xue Bao; 2008 Jul; 28(7):1210-3. PubMed ID: 18676265
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. 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]
34. 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]
35. Arrayed primer extension for the noninvasive prenatal diagnosis of beta-thalassemia based on detection of single nucleotide polymorphisms.
Papasavva T; Kalikas I; Kyrri A; Kleanthous M
Ann N Y Acad Sci; 2008 Aug; 1137():302-8. PubMed ID: 18837964
[TBL] [Abstract][Full Text] [Related]
36. Prenatal diagnosis of hemoglobinopathies in Hacettepe University, Turkey.
Beksac MS; Gumruk F; Gurgey A; Cakar N; Mumusoglu S; Ozyuncu O; Altay C
Pediatr Hematol Oncol; 2011 Feb; 28(1):51-5. PubMed ID: 20863160
[TBL] [Abstract][Full Text] [Related]
37. Non-invasive prenatal diagnostic testing for β-thalassaemia using cell-free fetal DNA and next generation sequencing.
Xiong L; Barrett AN; Hua R; Tan TZ; Ho SS; Chan JK; Zhong M; Choolani M
Prenat Diagn; 2015 Mar; 35(3):258-65. PubMed ID: 25400264
[TBL] [Abstract][Full Text] [Related]
38. Prenatal diagnosis using DNA polymorphisms. Report on 95 pregnancies at risk for sickle-cell disease or beta-thalassemia.
Boehm CD; Antonarakis SE; Phillips JA; Stetten G; Kazazian HH
N Engl J Med; 1983 May; 308(18):1054-8. PubMed ID: 6300677
[TBL] [Abstract][Full Text] [Related]
39. Rapid prenatal diagnosis of common beta-thalassemia mutations in Southeast Asia using pyrosequencing.
Ho SS; Huan PT; Leow GH; Ching LK; Chiu L; Law HY; Koay ES
Prenat Diagn; 2013 Nov; 33(11):1017-22. PubMed ID: 23794144
[TBL] [Abstract][Full Text] [Related]
40. Development of a PCR/LDR/capillary electrophoresis assay with potential for the detection of a beta-thalassemia fetal mutation in maternal plasma.
Yi P; Chen Z; Yu L; Zheng Y; Liu G; Xie H; Zhou Y; Zheng X; Han J; Li L
J Matern Fetal Neonatal Med; 2010 Aug; 23(8):920-7. PubMed ID: 20121392
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]