BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 31720905)

  • 1. Screening of triploid with low-coverage whole-genome sequencing by a single-nucleotide polymorphism-based test in miscarriage tissue.
    Geng Q; Cui X; Zhang Y; Zhang L; Zhang C; Wang K; Chen J; Zhu Q; Xie J; Xu Z; Liu Y; Zhang M; Ding L; Zhang W; Yang C
    J Assist Reprod Genet; 2019 Dec; 36(12):2525-2531. PubMed ID: 31720905
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysis.
    Levy B; Sigurjonsson S; Pettersen B; Maisenbacher MK; Hall MP; Demko Z; Lathi RB; Tao R; Aggarwal V; Rabinowitz M
    Obstet Gynecol; 2014 Aug; 124(2 Pt 1):202-209. PubMed ID: 25004334
    [TBL] [Abstract][Full Text] [Related]  

  • 3. High resolution global chromosomal aberrations from spontaneous miscarriages revealed by low coverage whole genome sequencing.
    Qi H; Xuan ZL; Du Y; Cai LR; Zhang H; Wen XH; Kong XD; Yang K; Mi Y; Fu XX; Cao SB; Wang J; Chen CJ; Liang JB
    Eur J Obstet Gynecol Reprod Biol; 2018 May; 224():21-28. PubMed ID: 29525519
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Diploid/triploid mixoploidy: A consequence of asymmetric zygotic segregation of parental genomes.
    Carson JC; Hoffner L; Conlin L; Parks WT; Fisher RA; Spinner N; Yatsenko SA; Bonadio J; Surti U
    Am J Med Genet A; 2018 Dec; 176(12):2720-2732. PubMed ID: 30302900
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Comprehensive genetic analysis in first or second trimester pregnancy loss using chromosomal microarray with single nucleotide polymorphism probes].
    Zhu L; Zhang H; Du Q; Sun X; Liu W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Jun; 39(6):576-580. PubMed ID: 35773758
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sequential application of copy number variation sequencing and quantitative fluorescence polymerase chain reaction in genetic analysis of miscarriage and stillbirth.
    Chen Q; Zhang H; Li X; Li J; Chen H; Liu L; Zhou S; Xu Z
    Mol Genet Genomic Med; 2023 Aug; 11(8):e2187. PubMed ID: 37073418
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Single-nucleotide polymorphism microarray detects molar pregnancies in 3% of miscarriages.
    Maisenbacher MK; Merrion K; Kutteh WH
    Fertil Steril; 2019 Oct; 112(4):700-706. PubMed ID: 31395308
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Diagnostic utility of microarray testing in pregnancy loss.
    Rosenfeld JA; Tucker ME; Escobar LF; Neill NJ; Torchia BS; McDaniel LD; Schultz RA; Chong K; Chitayat D
    Ultrasound Obstet Gynecol; 2015 Oct; 46(4):478-86. PubMed ID: 25846569
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comparative study of single-nucleotide polymorphism array and next generation sequencing based strategies on triploid identification in preimplantation genetic diagnosis and screen.
    Xu J; Niu W; Peng Z; Bao X; Zhang M; Wang L; Du L; Zhang N; Sun Y
    Oncotarget; 2016 Dec; 7(49):81839-81848. PubMed ID: 27833086
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A survey of undetected, clinically relevant chromosome abnormalities when replacing postnatal karyotyping by Whole Genome Sequencing.
    Hochstenbach R; van Binsbergen E; Schuring-Blom H; Buijs A; Ploos van Amstel HK
    Eur J Med Genet; 2019 Sep; 62(9):103543. PubMed ID: 30248410
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Chromosomal microarray analysis for the causes of miscarriage or stillbirth].
    Xiao Y; Shi P; Li D; Wang J; Li R; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Apr; 37(4):389-391. PubMed ID: 32219819
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Triploid pregnancy-Clinical implications.
    Massalska D; Bijok J; Kucińska-Chahwan A; Zimowski JG; Ozdarska K; Panek G; Roszkowski T
    Clin Genet; 2021 Oct; 100(4):368-375. PubMed ID: 34031868
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [Chromosomal abnormalities in spontaneous miscarriage specimens detected by combinatorial probe anchor synthesis-based high-throughput low coverage whole genome sequencing].
    Wang XH; Bai RF; Zhou Y; Dong H; Ji YP; Hou DX; Wu RGML; Yang XL; Ji XP
    Zhonghua Fu Chan Ke Za Zhi; 2019 Dec; 54(12):808-814. PubMed ID: 31874470
    [No Abstract]   [Full Text] [Related]  

  • 15. Development of a Chromosomal Microarray Test for the Detection of Abnormalities in Formalin-Fixed, Paraffin-Embedded Products of Conception Specimens.
    Gliem TJ; Aypar U
    J Mol Diagn; 2017 Nov; 19(6):843-847. PubMed ID: 28807814
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Single-nucleotide polymorphism-based chromosomal microarray analysis provides clues and insights into disease mechanisms.
    Daum H; Meiner V; Hacohen N; Zvi N; Eilat A; Drai-Hasid R; Yagel S; Zenvirt S; Frumkin A
    Ultrasound Obstet Gynecol; 2019 Nov; 54(5):655-660. PubMed ID: 30693591
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Detection of triploid, molar, and vanishing twin pregnancies by a single-nucleotide polymorphism-based noninvasive prenatal test.
    Curnow KJ; Wilkins-Haug L; Ryan A; Kırkızlar E; Stosic M; Hall MP; Sigurjonsson S; Demko Z; Rabinowitz M; Gross SJ
    Am J Obstet Gynecol; 2015 Jan; 212(1):79.e1-9. PubMed ID: 25447960
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Triploidy as a cause of failure in human reproduction].
    Wołczyński S; Kulikowski M; Szamatowicz M
    Ginekol Pol; 1993 Mar; 64(3):154-60. PubMed ID: 8359744
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Application of Restriction Site-Associated DNA Sequencing (RAD-Seq) for Copy Number Variation and Triploidy Detection in Human.
    He JC; Li SY; He WZ; Xian JJ; Ma XY; Wang YC; Zhang MC; Ye GX; Liang B; Xia Q; Li Q
    Cytogenet Genome Res; 2021; 161(8-9):406-413. PubMed ID: 34657031
    [TBL] [Abstract][Full Text] [Related]  

  • 20. From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability.
    Lindstrand A; Eisfeldt J; Pettersson M; Carvalho CMB; Kvarnung M; Grigelioniene G; Anderlid BM; Bjerin O; Gustavsson P; Hammarsjö A; Georgii-Hemming P; Iwarsson E; Johansson-Soller M; Lagerstedt-Robinson K; Lieden A; Magnusson M; Martin M; Malmgren H; Nordenskjöld M; Norling A; Sahlin E; Stranneheim H; Tham E; Wincent J; Ygberg S; Wedell A; Wirta V; Nordgren A; Lundin J; Nilsson D
    Genome Med; 2019 Nov; 11(1):68. PubMed ID: 31694722
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.