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 *

428 related articles for article (PubMed ID: 28152582)

  • 1. Contribution of maternal copy number variations to false-positive fetal trisomies detected by noninvasive prenatal testing.
    Zhou X; Sui L; Xu Y; Song Y; Qi Q; Zhang J; Zhu H; Sun H; Tian F; Xu M; Cram DS; Liu J
    Prenat Diagn; 2017 Apr; 37(4):318-322. PubMed ID: 28152582
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Maternal X chromosome copy number variations are associated with discordant fetal sex chromosome aneuploidies detected by noninvasive prenatal testing.
    Wang S; Huang S; Ma L; Liang L; Zhang J; Zhang J; Cram DS
    Clin Chim Acta; 2015 Apr; 444():113-6. PubMed ID: 25689220
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center.
    Lau TK; Cheung SW; Lo PS; Pursley AN; Chan MK; Jiang F; Zhang H; Wang W; Jong LF; Yuen OK; Chan HY; Chan WS; Choy KW
    Ultrasound Obstet Gynecol; 2014 Mar; 43(3):254-64. PubMed ID: 24339153
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
    Wang J; Chen L; Zhou C; Wang L; Xie H; Xiao Y; Zhu H; Hu T; Zhang Z; Zhu Q; Liu Z; Liu S; Wang H; Xu M; Ren Z; Yu F; Cram DS; Liu H
    Am J Obstet Gynecol; 2018 Sep; 219(3):287.e1-287.e18. PubMed ID: 29852155
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Noninvasive prenatal diagnosis of common fetal chromosomal aneuploidies by maternal plasma DNA sequencing.
    Lau TK; Chen F; Pan X; Pooh RK; Jiang F; Li Y; Jiang H; Li X; Chen S; Zhang X
    J Matern Fetal Neonatal Med; 2012 Aug; 25(8):1370-4. PubMed ID: 22070770
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Expanded noninvasive prenatal testing for fetal aneuploidy and copy number variations and parental willingness for invasive diagnosis in a cohort of 18,516 cases.
    Ge Y; Li J; Zhuang J; Zhang J; Huang Y; Tan M; Li W; Chen J; Zhou Y
    BMC Med Genomics; 2021 Apr; 14(1):106. PubMed ID: 33853619
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Detection of fetal copy number variants by non-invasive prenatal testing for common aneuploidies.
    Li R; Wan J; Zhang Y; Fu F; Ou Y; Jing X; Li J; Li D; Liao C
    Ultrasound Obstet Gynecol; 2016 Jan; 47(1):53-7. PubMed ID: 26033469
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Non-invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146,958 pregnancies.
    Zhang H; Gao Y; Jiang F; Fu M; Yuan Y; Guo Y; Zhu Z; Lin M; Liu Q; Tian Z; Zhang H; Chen F; Lau TK; Zhao L; Yi X; Yin Y; Wang W
    Ultrasound Obstet Gynecol; 2015 May; 45(5):530-8. PubMed ID: 25598039
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Combining Effects of Cell-Free Circulating Tumor DNA of Breast Tumor to the Noninvasive Prenatal Testing Results: A Simulating Investigation.
    Cai YH; Yao GY; Chen LJ; Gan HY; Ye CS; Yang XX
    DNA Cell Biol; 2018 Jul; 37(7):626-633. PubMed ID: 29957029
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical application of expanded noninvasive prenatal testing for fetal chromosome abnormalities in a cohort of 39,580 pregnancies.
    Chen Y; Lu L; Zhang Y; Wang F; Ni Y; Wang Q; Ying C
    Am J Med Genet A; 2022 May; 188(5):1426-1434. PubMed ID: 35107205
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Performance Evaluation of NIPT in Detection of Chromosomal Copy Number Variants Using Low-Coverage Whole-Genome Sequencing of Plasma DNA.
    Liu H; Gao Y; Hu Z; Lin L; Yin X; Wang J; Chen D; Chen F; Jiang H; Ren J; Wang W
    PLoS One; 2016; 11(7):e0159233. PubMed ID: 27415003
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Statistical Approach to Decreasing the Error Rate of Noninvasive Prenatal Aneuploid Detection caused by Maternal Copy Number Variation.
    Zhang H; Zhao YY; Song J; Zhu QY; Yang H; Zheng ML; Xuan ZL; Wei Y; Chen Y; Yuan PB; Yu Y; Li DW; Liang JB; Fan L; Chen CJ; Qiao J
    Sci Rep; 2015 Nov; 5():16106. PubMed ID: 26534864
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Confined placental origin of the circulating cell free fetal DNA revealed by a discordant non-invasive prenatal test result in a trisomy 18 pregnancy.
    Mao J; Wang T; Wang BJ; Liu YH; Li H; Zhang J; Cram D; Chen Y
    Clin Chim Acta; 2014 Jun; 433():190-3. PubMed ID: 24667696
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Investigation on combined copy number variation sequencing and cytogenetic karyotyping for prenatal diagnosis.
    Zhang J; Tang X; Hu J; He G; Wang J; Zhu Y; Zhu B
    BMC Pregnancy Childbirth; 2021 Jul; 21(1):496. PubMed ID: 34238233
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratory.
    Dheedene A; Sante T; De Smet M; Vanbellinghen JF; Grisart B; Vergult S; Janssens S; Menten B
    Prenat Diagn; 2016 Aug; 36(8):699-707. PubMed ID: 27176606
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Non invasive prenatal test (NIPT) in maternal blood by parallel massive sequencing. Initial experience in Mexican women and literature review].
    Hernández-Gómez M; Ramirez-Arroyo E; Meléndez-Hernández R; Garduño-Zaraza LM; Mayén-Molina DG
    Ginecol Obstet Mex; 2015 May; 83(5):277-88. PubMed ID: 26233973
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage.
    Liu S; Song L; Cram DS; Xiong L; Wang K; Wu R; Liu J; Deng K; Jia B; Zhong M; Yang F
    Ultrasound Obstet Gynecol; 2015 Oct; 46(4):472-7. PubMed ID: 25767059
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Noninvasive prenatal testing of fetal aneuploidies by massively parallel sequencing in a prospective Chinese population.
    Song Y; Liu C; Qi H; Zhang Y; Bian X; Liu J
    Prenat Diagn; 2013 Jul; 33(7):700-6. PubMed ID: 23703459
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants.
    Lefkowitz RB; Tynan JA; Liu T; Wu Y; Mazloom AR; Almasri E; Hogg G; Angkachatchai V; Zhao C; Grosu DS; McLennan G; Ehrich M
    Am J Obstet Gynecol; 2016 Aug; 215(2):227.e1-227.e16. PubMed ID: 26899906
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of a trisomy 7 mosaic case: CMA, CNV-seq, karyotyping, interphase FISH, and MS-MLPA, which technique to choose?
    Cong X; Zhang T; Li Z; Luo X; Hu L; Liu W
    BMC Pregnancy Childbirth; 2024 May; 24(1):338. PubMed ID: 38702634
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.