BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

229 related articles for article (PubMed ID: 35287566)

  • 1. 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]  

  • 2. Noninvasive Prenatal Diagnosis of Beta-Thalassemia Disease by Using Digital PCR Analysis of Cell-Free Fetal DNA in Maternal Plasma.
    Charoenkwan P; Traisrisilp K; Sirichotiyakul S; Phusua A; Sanguansermsri T; Tongsong T
    Fetal Diagn Ther; 2022; 49(11-12):468-478. PubMed ID: 36574763
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Droplet Digital PCR for Non-Invasive Prenatal Detection of Fetal Single-Gene Point Mutations in Maternal Plasma.
    D'Aversa E; Breveglieri G; Boutou E; Balassopoulou A; Voskaridou E; Pellegatti P; Guerra G; Scapoli C; Gambari R; Borgatti M
    Int J Mol Sci; 2022 Mar; 23(5):. PubMed ID: 35269962
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Non-invasive prenatal testing for fetal inheritance of maternal β-thalassaemia mutations using targeted sequencing and relative mutation dosage: a feasibility study.
    Xiong L; Barrett AN; Hua R; Ho S; Jun L; Chan K; Mei Z; Choolani M
    BJOG; 2018 Mar; 125(4):461-468. PubMed ID: 29211324
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. [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]  

  • 10. Molecular genetics and prenatal diagnosis of beta thalassemia to control transfusion dependent births in carrier Pakistani couples.
    Kanwal S; Bukhari S; Perveen S
    J Pak Med Assoc; 2017 Jul; 67(7):1030-1034. PubMed ID: 28770881
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. High-resolution melting analysis for noninvasive prenatal diagnosis of IVS-II-I (G-A) fetal DNA in minor beta-thalassemia mothers.
    Zafari M; Gill P; Kowsaryan M; Alipour A; Banihashemi A
    J Matern Fetal Neonatal Med; 2016 Oct; 29(20):3323-8. PubMed ID: 26600408
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diagnostic Value of Non-Invasive Prenatal Screening of β-thalassemia by Cell Free Fetal DNA and Fetal NRBC.
    Shafei N; Hakhamaneshi MS; Houshmand M; Gerayeshnejad S; Fathi F; Sharifzadeh S
    Curr Mol Med; 2019; 19(2):105-111. PubMed ID: 30813874
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Noninvasive prenatal screening test for compound heterozygous beta thalassemia using an amplification refractory mutation system real-time polymerase chain reaction technique.
    Suwannakhon N; Pangeson T; Seeratanachot T; Mahingsa K; Pingyod A; Bumrungpakdee W; Sanguansermsri T
    Hematol Rep; 2019 Sep; 11(3):8124. PubMed ID: 31579144
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of beta-thalassemia: 12 years' experience at a single laboratory in Pakistan.
    Ahmed S
    Prenat Diagn; 2007 Dec; 27(13):1224-7. PubMed ID: 17987604
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Prenatal diagnosis of beta-thalassemia in Southern Punjab, Pakistan.
    Baig SM; Azhar A; Hassan H; Baig JM; Aslam M; Ud Din MA; Qureshi JA; Zaman T
    Prenat Diagn; 2006 Oct; 26(10):903-5. PubMed ID: 16821247
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Simultaneous detection of fetal aneuploidy, de novo FGFR3 mutations and paternally derived β-thalassemia by a novel method of noninvasive prenatal testing.
    Yang L; Wu Y; Hu Z; Zhang H; Pu D; Yan H; Zhang S; Jiang H; Liu Q; Yuan Y; Zhang Y; Chen F; Lu Y; Pan S; Lin L; Gao Y
    Prenat Diagn; 2021 Mar; 41(4):440-448. PubMed ID: 33340121
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.