BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 30593129)

  • 1. Invasive molecular prenatal diagnosis of alpha and beta thalassemia among Hakka pregnant women.
    Wu H; Wang H; Lan L; Zeng M; Guo W; Zheng Z; Zhu H; Wu J; Zhao P
    Medicine (Baltimore); 2018 Dec; 97(52):e13557. PubMed ID: 30593129
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
    Zhu BS; He J; Zhang J; Zeng XH; Su J; Xu XH; Li SY; Chen H; Zhang YH
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system.
    Karnpean R; Fucharoen G; Fucharoen S; Sae-ung N; Sanchaisuriya K; Ratanasiri T
    Acta Haematol; 2009; 121(4):227-33. PubMed ID: 19546525
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Molecular prenatal diagnosis of thalassemia in Taiwan.
    Chern SR; Chen CP
    Int J Gynaecol Obstet; 2000 May; 69(2):103-6. PubMed ID: 10802076
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Invasive prenatal diagnosis of α-thalassemia to control Hb Bart's hydrops fetalis syndrome: 15 years of experience.
    Lai K; Li S; Lin W; Yang D; Chen W; Li M; Pang L; Chen P
    Arch Gynecol Obstet; 2018 Aug; 298(2):307-311. PubMed ID: 29948167
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diagnostic value of fetal hemoglobin Bart's for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy.
    Singha K; Yamsri S; Chaibunruang A; Srivorakun H; Sanchaisuriya K; Fucharoen G; Fucharoen S
    Orphanet J Rare Dis; 2022 Feb; 17(1):45. PubMed ID: 35144630
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [A community-based genetic screening of large-scale population and prenatal diagnosis for alpha and beta thalassemia in Zhuhai city of Guangdong province].
    Zhou YQ; Mo QH; Lu JH; Li LY; Liang X; Jia SQ; Xiao GF; Zhou WJ; Xiao QZ; Xu XM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Jun; 25(3):256-61. PubMed ID: 18543211
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A Pilot Study of Noninvasive Prenatal Diagnosis of Alpha- and Beta-Thalassemia with Target Capture Sequencing of Cell-Free Fetal DNA in Maternal Blood.
    Wang W; Yuan Y; Zheng H; Wang Y; Zeng D; Yang Y; Yi X; Xia Y; Zhu C
    Genet Test Mol Biomarkers; 2017 Jul; 21(7):433-439. PubMed ID: 28537755
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. [Prenatal diagnosis of Thailand deletion of α-thalassemia 1 families].
    Lin N; Lin Y; Huang HL; Lin XL; He DQ; He SQ; Guo DH; Li Y; Xu LP
    Zhonghua Yi Xue Za Zhi; 2016 Jun; 96(24):1919-22. PubMed ID: 27373361
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of alpha-thalassemia in beta-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening.
    Li D; Liao C; Li J; Xie X; Huang Y; Zhong H
    Haematologica; 2006 May; 91(5):649-51. PubMed ID: 16627247
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analysis of real-time PCR cycle threshold of alpha-thalassemia-1 Southeast Asian type deletion using fetal cell-free DNA in maternal plasma for noninvasive prenatal diagnosis of Bart's hydrops fetalis.
    Pornprasert S; Sukunthamala K; Kunyanone N; Sittiprasert S; Thungkham K; Junorse S; Pongsawatkul K; Pattanaporn W; Jitwong C; Sanguansermsri T
    J Med Assoc Thai; 2010 Nov; 93(11):1243-8. PubMed ID: 21114201
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [A rare thalassemia intermedia case caused by co-existence of Hb H disease (--(SEA)/-alpha(4.2)) and beta-thalassemia major (beta (CD17A)>T/beta (IVS2-654C)>T): implications for prenatal diagnosis].
    Li Q; Li LY; Mo QH
    Nan Fang Yi Ke Da Xue Xue Bao; 2008 Jan; 28(1):16-9. PubMed ID: 18227017
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prevalence and molecular spectrum of α- and β-globin gene mutations in Hainan, China.
    Wang Z; Sun W; Chen H; Zhang Y; Wang F; Chen H; Zhou Y; Huang Y; Zhou X; Li Q; Ma Y
    Int J Hematol; 2021 Sep; 114(3):307-318. PubMed ID: 34195938
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Prenatal diagnosis of Thailand deletion of alpha-thalassemia 1].
    Chen P; Li SQ; Li MQ; Pang LH; Lin WX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):247-50. PubMed ID: 17557230
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular analysis of hemoglobinopathies in a large ethnic Hakka population in southern China.
    Zhao P; Wu H; Weng R
    Medicine (Baltimore); 2018 Nov; 97(45):e13034. PubMed ID: 30407298
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of Hb Bart's hydrops fetalis caused by a genetic compound heterozygosity for two different alpha-thalassemia determinants.
    Siriratmanawong N; Pinmuang-Ngam C; Fucharoen G; Fucharoen S
    Fetal Diagn Ther; 2007; 22(4):264-8. PubMed ID: 17369692
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.