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 *

134 related articles for article (PubMed ID: 38603985)

  • 1. Prenatal chromosomal microarray analysis and karyotyping in fetuses with isolated choroid plexus cyst: A retrospective case-control study.
    Wang L; Liang P; Pan P; Su J; Qin J; Chen Z; Huang D; Sun W; Song P; Wei H
    Eur J Obstet Gynecol Reprod Biol; 2024 Jun; 297():91-95. PubMed ID: 38603985
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomalies.
    Li L; He Z; Huang X; Lin S; Wu J; Huang L; Wan Y; Fang Q
    Ultrasound Obstet Gynecol; 2020 Apr; 55(4):502-509. PubMed ID: 30977228
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Application of chromosomal microarray analysis for fetuses with choroid plexus cysts].
    Jin K; Zhang J; Xu X; Zhang L; Yang Y; Shen S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Dec; 39(12):1334-1338. PubMed ID: 36453954
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal detection of chromosomal abnormalities and copy number variants in fetuses with ventriculomegaly.
    Chang Q; Yang Y; Peng Y; Liu S; Li L; Deng X; Yang M; Lan Y
    Eur J Paediatr Neurol; 2020 Mar; 25():106-112. PubMed ID: 32014392
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association of prenatal renal ultrasound abnormalities with pathogenic copy number variants in a large Chinese cohort.
    Su J; Qin Z; Fu H; Luo J; Huang Y; Huang P; Zhang S; Liu T; Lu W; Li W; Jiang T; Wei S; Yang S; Shen Y
    Ultrasound Obstet Gynecol; 2022 Feb; 59(2):226-233. PubMed ID: 34090309
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Application of single nucleotide polymorphism array in prenatal diagnosis for fetuses with abnormal ultrasound findings].
    Guo YL; Wang L; Xue SW; Qu SZ; Yang J; Xu H; Bai ZX; Liu N; Kong XD
    Zhonghua Fu Chan Ke Za Zhi; 2018 Jul; 53(7):464-470. PubMed ID: 30078256
    [No Abstract]   [Full Text] [Related]  

  • 7. Prenatal diagnosis of fetuses with absent/hypoplastic nasal bone in second-trimester using chromosomal microarray analysis.
    Chen X; Jiang Y; Zeng S; Zhuang J; Lin N
    Birth Defects Res; 2024 May; 116(5):e2351. PubMed ID: 38766695
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing.
    Shi X; Tang H; Lu J; Yang X; Ding H; Wu J
    Ann Med; 2021 Dec; 53(1):1285-1291. PubMed ID: 34374610
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies.
    Sagi-Dain L; Cohen Vig L; Kahana S; Yacobson S; Tenne T; Agmon-Fishman I; Klein C; Matar R; Basel-Salmon L; Maya I
    Genet Med; 2019 Nov; 21(11):2462-2467. PubMed ID: 31123319
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype.
    Su L; Huang H; An G; Cai M; Wu X; Li Y; Xie X; Lin Y; Wang M; Xu L
    Mol Genet Genomic Med; 2019 Aug; 7(8):e811. PubMed ID: 31209990
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Application of chromosomal microarray in fetuses with increased nuchal translucency.
    Zhao XR; Gao L; Wu Y; Wang YL
    J Matern Fetal Neonatal Med; 2020 May; 33(10):1749-1754. PubMed ID: 30688128
    [No Abstract]   [Full Text] [Related]  

  • 13. Detection of submicroscopic chromosomal aberrations by chromosomal microarray analysis for the prenatal diagnosis of central nervous system abnormalities.
    Song T; Xu Y; Li Y; Jia L; Zheng J; Dang Y; Wan S; Zheng Y; Zhang J; Yang H
    J Clin Lab Anal; 2020 Oct; 34(10):e23434. PubMed ID: 32677110
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The clinical use of chromosomal microarray analysis in detection of fetal chromosomal rearrangements: a study from China Mainland.
    Wu Y; Wang Y; Tao J; Han X; Zhao X; Liu C; Gao L; Cheng W
    Eur J Obstet Gynecol Reprod Biol; 2017 May; 212():44-50. PubMed ID: 28340467
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Clinical Experience of Prenatal Chromosomal Microarray Analysis in 6159 Ultrasonically Abnormal Fetuses.
    Song T; Xu Y; Li Y; Zheng J; Guo F; Jin X; Li J; Zhang J; Yang H
    Reprod Sci; 2024 Apr; 31(4):1089-1107. PubMed ID: 38012523
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Bayesian risk analysis for Trisomy 21 in isolated choroid plexus cyst: combining a prenatal database with a meta-analysis.
    Kürten C; Knippel A; Verde P; Kozlowski P
    J Matern Fetal Neonatal Med; 2021 Mar; 34(6):889-897. PubMed ID: 31113245
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of fetuses conceived by assisted reproductive technology by karyotyping and chromosomal microarray analysis.
    Guo H; Sheng R; Zhang X; Jin X; Gu W; Liu T; Dong H; Jia R
    PeerJ; 2023; 11():e14678. PubMed ID: 36684682
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis and pregnancy outcomes of fetuses with polyhydramnios.
    Liu Y; Hu T; Qian Y; Wang J; Hu R; Xiao L; Liao N; Liu Z; Wang H; Liu S; Zhang Z
    J Matern Fetal Neonatal Med; 2024 Dec; 37(1):2344089. PubMed ID: 38710614
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.
    Hillman SC; McMullan DJ; Hall G; Togneri FS; James N; Maher EJ; Meller CH; Williams D; Wapner RJ; Maher ER; Kilby MD
    Ultrasound Obstet Gynecol; 2013 Jun; 41(6):610-20. PubMed ID: 23512800
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.