These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 29266293)

  • 21. Prenatal screening for and diagnosis of aneuploidy in twin pregnancies.
    Audibert F; Gagnon A; ;
    J Obstet Gynaecol Can; 2011 Jul; 33(7):754-67. PubMed ID: 21749753
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Nationwide demonstration project of next-generation sequencing of cell-free DNA in maternal plasma in Japan: 1-year experience.
    Sago H; Sekizawa A;
    Prenat Diagn; 2015 Apr; 35(4):331-6. PubMed ID: 25408438
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Noninvasive prenatal diagnosis using next-generation sequencing.
    Xu L; Shi R
    Gynecol Obstet Invest; 2014; 77(2):73-7. PubMed ID: 24192219
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Introducing WISECONDOR for noninvasive prenatal diagnostics.
    Straver R; Sistermans EA; Reinders MJ
    Expert Rev Mol Diagn; 2014 Jun; 14(5):513-5. PubMed ID: 24831532
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Validation of Extensive Next-Generation Sequencing Method for Monogenic Disorder Analysis on Cell-Free Fetal DNA: Noninvasive Prenatal Diagnosis.
    Dello Russo C; Cesta A; Longo S; Barone MA; Cima A; Mesoraca A; Sparacino D; Viola A; Giorlandino C
    J Mol Diagn; 2019 Jul; 21(4):572-579. PubMed ID: 31028936
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The promise of non-invasive prenatal testing needs to be monitored scientifically.
    Lonardo F; Scarano G
    BMJ; 2015 May; 350():h2518. PubMed ID: 25975672
    [No Abstract]   [Full Text] [Related]  

  • 27. Fetal Genotyping in Maternal Blood by Digital PCR: Towards NIPD of Monogenic Disorders Independently of Parental Origin.
    Perlado S; Bustamante-Aragonés A; Donas M; Lorda-Sánchez I; Plaza J; Rodríguez de Alba M
    PLoS One; 2016; 11(4):e0153258. PubMed ID: 27078875
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Noninvasive prenatal diagnosis of fetal aneuploidies and Mendelian disorders: new innovative strategies.
    Hahn S; Jackson LG; Kolla V; Mahyuddin AP; Choolani M
    Expert Rev Mol Diagn; 2009 Sep; 9(6):613-21. PubMed ID: 19732005
    [TBL] [Abstract][Full Text] [Related]  

  • 29. #36: Prenatal aneuploidy screening using cell-free DNA.
    Society for Maternal-Fetal Medicine (SMFM) Publications Committee. Electronic address: pubs@smfm.org
    Am J Obstet Gynecol; 2015 Jun; 212(6):711-6. PubMed ID: 25813012
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cell-Free DNA Screening: Complexities and Challenges of Clinical Implementation.
    Grace MR; Hardisty E; Dotters-Katz SK; Vora NL; Kuller JA
    Obstet Gynecol Surv; 2016 Aug; 71(8):477-87. PubMed ID: 27526871
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Noninvasive Prenatal Diagnosis for Cystic Fibrosis: Implementation, Uptake, Outcome, and Implications.
    Chandler NJ; Ahlfors H; Drury S; Mellis R; Hill M; McKay FJ; Collinson C; Hayward J; Jenkins L; Chitty LS
    Clin Chem; 2020 Jan; 66(1):207-216. PubMed ID: 31551312
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Towards a generalization of non-invasive prenatal diagnosis of single-gene disorders? Assesment and outlook].
    Verebi C; Gravrand V; Pacault M; Audrezet MP; Couque N; Vincent MC; Leturcq F; Tsatsaris V; Bienvenu T; Nectoux J
    Gynecol Obstet Fertil Senol; 2023 Oct; 51(10):463-470. PubMed ID: 37517661
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Advances in the prenatal diagnosis of monogenic disorders.
    Chitty LS
    Prenat Diagn; 2018 Jan; 38(1):3-5. PubMed ID: 29464795
    [No Abstract]   [Full Text] [Related]  

  • 34. The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress made.
    Lench N; Barrett A; Fielding S; McKay F; Hill M; Jenkins L; White H; Chitty LS
    Prenat Diagn; 2013 Jun; 33(6):555-62. PubMed ID: 23592512
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Non-invasive prenatal testing is a breakthrough in prenatal screening].
    Hornstrup LS; Ambye L; Sørensen S; Jørgensen FS
    Ugeskr Laeger; 2015 Jul; 177(28):. PubMed ID: 26239855
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Clinical perspective of cell-free DNA testing for fetal aneuploidies.
    Gratacós E; Nicolaides K
    Fetal Diagn Ther; 2014; 35(3):151-5. PubMed ID: 24931002
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A Novel Targeted Approach for Noninvasive Detection of Paternally Inherited Mutations in Maternal Plasma.
    van den Oever JM; van Minderhout IJ; Harteveld CL; den Hollander NS; Bakker E; van der Stoep N; Boon EM
    J Mol Diagn; 2015 Sep; 17(5):590-6. PubMed ID: 26162331
    [TBL] [Abstract][Full Text] [Related]  

  • 38. New tools for an old quest.
    Weiner CP
    Am J Obstet Gynecol; 2013 May; 208(5):339-40. PubMed ID: 23280393
    [No Abstract]   [Full Text] [Related]  

  • 39. Droplet digital PCR, a new approach to analyze fetal DNA from maternal blood: application to the determination of fetal RHD genotype.
    Orhant L; Rondeau S; Vasson A; Anselem O; Goffinet F; Allach El Khattabi L; Leturcq F; Vidaud D; Bienvenu T; Tsatsaris V; Nectoux J
    Ann Biol Clin (Paris); 2016 Jun; 74(3):269-77. PubMed ID: 27237800
    [TBL] [Abstract][Full Text] [Related]  

  • 40. An Overview on Prenatal Screening for Chromosomal Aberrations.
    Hixson L; Goel S; Schuber P; Faltas V; Lee J; Narayakkadan A; Leung H; Osborne J
    J Lab Autom; 2015 Oct; 20(5):562-73. PubMed ID: 25587000
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.