BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 33340121)

  • 21. Development of Reference Materials for Noninvasive Prenatal Aneuploidy Testing by Massively Parallel Sequencing: A Proof-of-Concept Study.
    Blais J; Giroux S; Caron A; Clément V; Rousseau F
    J Appl Lab Med; 2019 Jul; 4(1):50-60. PubMed ID: 31639707
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Establishing and validating noninvasive prenatal testing procedure for fetal aneuploidies in Vietnam.
    Phan MD; Nguyen TV; Trinh HNT; Vo BT; Nguyen TM; Nguyen NH; Nguyen TTQ; Do TTT; Hoang TTD; Truong KD; Giang H; Nguyen HN
    J Matern Fetal Neonatal Med; 2019 Dec; 32(23):4009-4015. PubMed ID: 29865915
    [No Abstract]   [Full Text] [Related]  

  • 23. Performance of Cell-Free DNA Screening for Fetal Common Aneuploidies and Sex Chromosomal Abnormalities: A Prospective Study from a Less Developed Autonomous Region in Mainland China.
    Lai Y; Zhu X; He S; Dong Z; Tang Y; Xu F; Chen Y; Meng L; Tao Y; Yi S; Su J; Huang H; Luo J; Leung TY; Wei H
    Genes (Basel); 2021 Mar; 12(4):. PubMed ID: 33806256
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal Malignancies.
    Bianchi DW; Chudova D; Sehnert AJ; Bhatt S; Murray K; Prosen TL; Garber JE; Wilkins-Haug L; Vora NL; Warsof S; Goldberg J; Ziainia T; Halks-Miller M
    JAMA; 2015 Jul; 314(2):162-9. PubMed ID: 26168314
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Development and validation of a novel panel of 16 STR markers for simultaneous diagnosis of β-thalassemia, aneuploidy screening, maternal cell contamination detection and fetal sample authenticity in PND and PGD/PGS cases.
    Sharifi Z; Rahiminejad F; Joudaki A; Bandehi AS; Farahzadi H; Keshvar Y; Golnabi F; Naderi S; Yazdani R; Shafaat M; Ghadami S; Abiri M; Zeinali S
    Sci Rep; 2019 May; 9(1):7452. PubMed ID: 31092881
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Noninvasive Prenatal Test for β-Thalassemia and Sickle Cell Disease Using Probe Capture Enrichment and Next-Generation Sequencing of DNA in Maternal Plasma.
    Erlich HA; López-Peña C; Carlberg KT; Shih S; Bali G; Yamaguchi KD; Salamon H; Das R; Lal A; Calloway CD
    J Appl Lab Med; 2022 Mar; 7(2):515-531. PubMed ID: 34849992
    [TBL] [Abstract][Full Text] [Related]  

  • 27. An adaptive detection method for fetal chromosomal aneuploidy using cell-free DNA from 447 Korean women.
    Kim S; Jung H; Han SH; Lee S; Kwon J; Kim MG; Chu H; Han K; Kwak H; Park S; Joo HJ; An M; Ha J; Lee K; Kim BC; Zheng H; Zhu X; Chen H; Bhak J
    BMC Med Genomics; 2016 Oct; 9(1):61. PubMed ID: 27716407
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Development and clinical application of a preimplantation genetic testing for monogenic disease (PGT-M) for beta thalassemia in Vietnam.
    Mai AD; Harton GL; Quang VN; Van HN; Thi NH; Thuy NP; Le Thi TH; Minh DN; Quoc QT
    J Assist Reprod Genet; 2021 Feb; 38(2):365-374. PubMed ID: 33216308
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Validation of fetal DNA fraction estimation and its application in noninvasive prenatal testing for aneuploidy detection in multiple pregnancies.
    Chen M; Jiang F; Guo Y; Yan H; Wang J; Zhang L; Zeng X; Li S; Li Y; Li N; Zhang C; Zhu W; Du B; Wang Y; Lan Z; Luo X; Luo F; Chen D
    Prenat Diagn; 2019 Dec; 39(13):1273-1282. PubMed ID: 31671222
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Efficiency of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies.
    Shi Y; Li X; Ju D; Li Y; Zhang X; Zhang Y
    Gynecol Obstet Invest; 2021; 86(4):379-387. PubMed ID: 34384080
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Combining the use of a fetal fraction-based risk algorithm and probability of an informative redraw in noninvasive prenatal testing for fetal aneuploidy.
    Benn P; Martin K; McKanna T; Valenti E; Billings P; Demko Z
    J Genet Couns; 2020 Oct; 29(5):800-806. PubMed ID: 31872514
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Detection of a de novo Y278C mutation in FGFR3 in a pregnancy with severe fetal hypochondroplasia: prenatal diagnosis and literature review.
    Chen CP; Su YN; Lin TH; Chang TY; Su JW; Wang W
    Taiwan J Obstet Gynecol; 2013 Dec; 52(4):580-5. PubMed ID: 24411048
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Screening of fetal chromosomal aneuploidy diseases using noninvasive prenatal testing in twin pregnancies.
    Yu W; Lv Y; Yin S; Liu H; Li X; Liang B; Kong L; Liu C
    Expert Rev Mol Diagn; 2019 Feb; 19(2):189-196. PubMed ID: 30582381
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A two-year experience of non-invasive prenatal testing (NIPT) at an urban tertiary medical center in South Korea.
    Noh JJ; Ryu HM; Oh SY; Choi SJ; Roh CR; Kim JH
    Taiwan J Obstet Gynecol; 2019 Jul; 58(4):545-551. PubMed ID: 31307749
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Non invasive prenatal testing (NIPT) for common aneuploidies and beyond.
    Alberry MS; Aziz E; Ahmed SR; Abdel-Fattah S
    Eur J Obstet Gynecol Reprod Biol; 2021 Mar; 258():424-429. PubMed ID: 33550217
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Predicting fetoplacental mosaicism during cfDNA-based NIPT.
    Neofytou M
    Curr Opin Obstet Gynecol; 2020 Apr; 32(2):152-158. PubMed ID: 31977337
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [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]  

  • 39. 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]  

  • 40. [Not Available].
    Žilina O; Rekker K; Kaplinski L; Sauk M; Paluoja P; Teder H; Ustav EL; Tõnisson N; Reimand T; Ridnõi K; Palta P; Vermeesch JR; Krjutškov K; Kurg A; Salumets A
    Prenat Diagn; 2019 Dec; 39(13):1262-1268. PubMed ID: 31691324
    [TBL] [Abstract][Full Text] [Related]  

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