219 related articles for article (PubMed ID: 31036126)
21. Non-invasive prenatal diagnosis using fetal DNA in maternal plasma: a preliminary study for identification of paternally-inherited alleles using single nucleotide polymorphisms.
Chen JJ; Tan JA; Chua KH; Tan PC; George E
BMJ Open; 2015 Jul; 5(7):e007648. PubMed ID: 26201722
[TBL] [Abstract][Full Text] [Related]
22. Molecular prenatal diagnosis of alpha and beta thalassemia in pregnant Hakka women in southern China.
Zhao P; Wu H; Zhong Z; Lan L; Zeng M; Lin H; Wang H; Zheng Z; Su L; Guo W
J Clin Lab Anal; 2018 Mar; 32(3):. PubMed ID: 28771834
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. [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]
26. Development of new substrates for high-sensitive genotyping of minority mutated alleles.
Galbiati S; Damin F; Di Carlo G; Ferrari M; Cremonesi L; Chiari M
Electrophoresis; 2008 Dec; 29(23):4714-22. PubMed ID: 19053069
[TBL] [Abstract][Full Text] [Related]
27. Isolation and analysis of cell-free fetal DNA from maternal peripheral blood in Chinese women.
Yang WC; Zhu L; Qiu YM; Zhou BX; Cheng JL; Wei CL; Chen HC; Li LY; Fu XD; Fu JJ
Genet Mol Res; 2015 Dec; 14(4):18078-89. PubMed ID: 26782455
[TBL] [Abstract][Full Text] [Related]
28. Noninvasive prenatal testing of beta-thalassemia for common Pakistani mutations: a comparative study using cell-free fetal DNA from maternal plasma and chorionic villus sampling.
Afzal M; Naeem MA; Ahmed S; Amin N; Rahim A; Munawar M; Ishaq M; Rathore A; Maria K
Hematology; 2022 Dec; 27(1):353-359. PubMed ID: 35287566
[TBL] [Abstract][Full Text] [Related]
29. β-Thalassemia mutations found during 1 year of prenatal diagnoses in Fars Province, Iran.
Rahiminejad MS; Zeinali S; Afrasiabi A; Valeshabad AK
Hemoglobin; 2011; 35(4):331-7. PubMed ID: 21797700
[TBL] [Abstract][Full Text] [Related]
30. Non‑invasive prenatal diagnosis of thalassemia through multiplex PCR, target capture and next‑generation sequencing.
Yang X; Ye Y; Fan D; Lin S; Li M; Hou H; Zhang J; Yang X
Mol Med Rep; 2020 Aug; 22(2):1547-1557. PubMed ID: 32627040
[TBL] [Abstract][Full Text] [Related]
31. [Non-invasive prenatal diagnosis for beta-thalassemia by detecting paternal CD41-42 mutation in cell-free DNA derived from maternal plasma with droplet digital PCR].
Zhang Y; Gong X; He Y; Huang L; Zhang Q; Liu Y; Li J; Chen Y; Zhou W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Dec; 35(6):787-790. PubMed ID: 30512146
[TBL] [Abstract][Full Text] [Related]
32. [Genetic Diagnosis of Thalassemia in Baise, Guangxi Zhuang Autonomous Region].
Lu H; Qin Q; Li JH; Chen T; Liang SJ; Lu XS
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2021 Jun; 29(3):865-868. PubMed ID: 34105485
[TBL] [Abstract][Full Text] [Related]
33. Prenatal diagnosis of beta-thalassemia major by high-performance liquid chromatography analysis of hemoglobins in fetal blood samples.
Sanguansermsri T; Thanarattanakorn P; Steger HF; Tongsong T; Chanprapaph P; Wanpirak C; Siriwatanapa P; Sirichotiyakul S; Flatz G
Hemoglobin; 2001 Feb; 25(1):19-27. PubMed ID: 11300346
[TBL] [Abstract][Full Text] [Related]
34. [Genetic diagnosis of thalassemia mutations with free fetal DNA in pregnant plasma].
Lin XR; You LX; Chen Y
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2013 Oct; 21(5):1215-9. PubMed ID: 24156437
[TBL] [Abstract][Full Text] [Related]
35. Detection of Paternal IVS-II-1 (G>A) (
Mortazavipour MM; Shahbazi S; Mahdian R
Hemoglobin; 2020 May; 44(3):168-173. PubMed ID: 32703054
[TBL] [Abstract][Full Text] [Related]
36. Prenatal exclusion of beta thalassaemia major by examination of maternal plasma.
Chiu RW; Lau TK; Leung TN; Chow KC; Chui DH; Lo YM
Lancet; 2002 Sep; 360(9338):998-1000. PubMed ID: 12383672
[TBL] [Abstract][Full Text] [Related]
37. [Large-scale population-based genetic screening and prenatal diagnosis for thalassemias in Zhuhai City of Guangdong Province].
Zhou YQ; Shang X; Yin BM; Xiong F; Xiao QZ; Zhou WJ; Zhang YL; Xu XM
Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):90-5. PubMed ID: 22455738
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. 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]
40. Prenatal screening of single-gene disorders from maternal blood.
Sekizawa A; Saito H
Am J Pharmacogenomics; 2001; 1(2):111-7. PubMed ID: 12174672
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]