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 *

169 related articles for article (PubMed ID: 37102283)

  • 1. [The value of chromosomal microarray analysis and fluorescence in situ hybridization for the prenatal diagnosis of chromosomal mosaicisms].
    Zheng J; An N; Li M; Xu M; Guan Y; Liu J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 May; 40(5):527-531. PubMed ID: 37102283
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Assessment of Combined Karyotype Analysis and Chromosome Microarray Analysis in Prenatal Diagnosis: A Cohort Study of 3710 Pregnancies.
    Wang J; Wang D; Yin Y; Deng Y; Ye M; Wei P; Zhang Z; Chen C; Qin S; Wang X
    Genet Res (Camb); 2022; 2022():6791439. PubMed ID: 36636555
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Comparison of performance of two prenatal diagnostic techniques for the detection of chromosomal mosaicisms in amniocytes].
    Sun W; Su J; Liu T; Huang H; Ouyang L; Wang L; Li J; Luo J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Aug; 39(8):842-847. PubMed ID: 35929933
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal Diagnosis of Chromosomal Mosaicism in 18,369 Cases of Amniocentesis.
    Kang H; Wang L; Xie Y; Chen Y; Gao C; Li X; Hu Y; Liu Q
    Am J Perinatol; 2024 May; 41(S 01):e2058-e2068. PubMed ID: 37336233
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [The value of combined CNV-Seq and chromosomal karyotyping for the detection of amniocytic mosaicisms and a literature review].
    Shi P; Zhu R; Zhao J; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):954-959. PubMed ID: 37532494
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Application of different technologies for distinguishing true and pseudo mosaicisms during prenatal diagnosis].
    Zhu R; Zhu X; Yang Y; Duan H; Zhang Y; Wu X; Wang W; Li J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):636-40. PubMed ID: 25297599
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [The value of combined use of chromosomal karyotyping and chromosome microarray analysis for prenatal diagnosis].
    Rao H; Liu Y; Lu Q; Huang N; Zhou J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Apr; 37(4):392-396. PubMed ID: 32219820
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Fetal mosaicism, should conventional karyotype always be performed?
    Su L; Wu X; Liang B; Lin N; Xie X; Cai M; Zheng L; Wang M; Xu L
    J Obstet Gynaecol Res; 2023 Dec; 49(12):2836-2848. PubMed ID: 37844871
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].
    Ulmer R; Pfeiffer RA; Kollert A; Beinder E
    Z Geburtshilfe Neonatol; 2000; 204(1):1-7. PubMed ID: 10721179
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Comparison of detection rates of chromosome G-banding karyotype analysis and fluorescence in situ hybridization among children with sex chromosome mosaicisms].
    Xiao W; Huang J; Liu W; Li B; Su Z; Pan L; Chen Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Jan; 40(1):12-16. PubMed ID: 36584993
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Combined chromosomal microarray analysis and fluorescence in situ hybridization for prenatal diagnosis of two cases with Pallister-Killian syndrome].
    Wang T; Ren C; Guo L; Lu J; Chen H; Huang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Jun; 36(6):571-573. PubMed ID: 31055807
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Report content and prenatal diagnosis of non-invasive prenatal testing for sex chromosome aneuploidy].
    Zhou CX; He LL; Zhu XY; Li ZX; Duan HL; Liu W; Gu LL; Li J
    Zhonghua Fu Chan Ke Za Zhi; 2023 Oct; 58(10):766-773. PubMed ID: 37849257
    [No Abstract]   [Full Text] [Related]  

  • 13. [Accidental discovery of copy number variation on chromosome 1 in a fetus with high risk of trisomy 13 suggested by NIPT].
    Chang J; Song Y; Qi Q; Hao N; Liu J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):922-927. PubMed ID: 37532489
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The difference between karyotype analysis and chromosome microarray for mosaicism of aneuploid chromosomes in prenatal diagnosis.
    Hao M; Li L; Zhang H; Li L; Liu R; Yu Y
    J Clin Lab Anal; 2020 Dec; 34(12):e23514. PubMed ID: 32864771
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Clinical features and genetic analysis of two fetuses with ring chromosome 21 mosaicism].
    Ji Y; Xu Y; Sun L; Ge Y; Cai M; Wu Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):1032-1035. PubMed ID: 37532507
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Prenatal diagnosis of fetal microdeletion and microduplication syndromes among pregnant women with advanced maternal ages].
    Duan F; Wu Q; Xu Y; Sun S; Ji Y; Sun L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Apr; 41(4):486-493. PubMed ID: 38565517
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].
    Zhang YP; Wu JP; Li XT; Lei CX; Xu JZ; Yin M
    Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):644-8. PubMed ID: 22176986
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis.
    Mademont-Soler I; Morales C; Soler A; Martínez-Crespo JM; Shen Y; Margarit E; Clusellas N; Obón M; Wu BL; Sánchez A
    Ultrasound Obstet Gynecol; 2013 Apr; 41(4):375-82. PubMed ID: 23233332
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Concordance of Chromosomal Microarray Analysis in Prenatal Diagnosis of Fetuses with Abnormal Ultrasonographic Soft Markers.
    Lu Y; Liu C; Ji Y
    J Coll Physicians Surg Pak; 2023 Mar; 33(3):270-274. PubMed ID: 36945155
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of BACs-on-Beads assay in 1520 cases from Fujian Province, China.
    Wang Y; Zhang M; Chen L; Huang H; Xu L
    Mol Genet Genomic Med; 2020 Oct; 8(10):e1446. PubMed ID: 32767744
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.