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 *

150 related articles for article (PubMed ID: 35928088)

  • 21. Submicroscopic chromosomal abnormalities in fetuses with increased nuchal translucency and normal karyotype.
    Yang X; Li R; Fu F; Zhang Y; Li D; Liao C
    J Matern Fetal Neonatal Med; 2017 Jan; 30(2):194-198. PubMed ID: 26998667
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Whole exome sequencing as a diagnostic adjunct to clinical testing in fetuses with structural abnormalities.
    Fu F; Li R; Li Y; Nie ZQ; Lei T; Wang D; Yang X; Han J; Pan M; Zhen L; Ou Y; Li J; Li FT; Jing X; Li D; Liao C
    Ultrasound Obstet Gynecol; 2018 Apr; 51(4):493-502. PubMed ID: 28976722
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Application of next-generation DNA sequencing for prenatal testing of fetal chromosomal aneuploidies].
    Liu J; Wang H; Xi H; Jia Z; Zhou Y; Wu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Aug; 32(4):533-7. PubMed ID: 26252102
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Prospective cohort study of fetal nuchal translucency in first-trimester and pregnancy outcome].
    Tang HR; Zhang Y; Ru T; Li J; Yang L; Xu Y; Duan HL; Wang Y; Wang Y; Hu YL; Zhang Y; Zheng MM
    Zhonghua Fu Chan Ke Za Zhi; 2020 Feb; 55(2):94-99. PubMed ID: 32146737
    [No Abstract]   [Full Text] [Related]  

  • 25. Chromosomal abnormalities not currently detected by cell-free fetal DNA: a retrospective analysis at a single center.
    Shani H; Goldwaser T; Keating J; Klugman S
    Am J Obstet Gynecol; 2016 Jun; 214(6):729.e1-729.e11. PubMed ID: 26721783
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype.
    Wu X; Li Y; Su L; Xie X; Cai M; Lin N; Huang H; Lin Y; Xu L
    Mol Diagn Ther; 2020 Oct; 24(5):611-619. PubMed ID: 32651932
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cytogenetic Analysis of Amniotic Fluid Cells in 4206 Cases of High-Risk Pregnant Women.
    Li H; Li Y; Zhao R; Zhang Y
    Iran J Public Health; 2019 Jan; 48(1):126-131. PubMed ID: 30847320
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Cytogenetic Investigation in 136 Consecutive Stillbirths: Does the Tissue Type Affect the Success Rate of Chromosomal Microarray Analysis and Karyotype?
    Marquès B; Benitez L; Peguero A; Madrigal I; Gómez O; Figueras F; Borrell A
    Fetal Diagn Ther; 2020; 47(4):315-320. PubMed ID: 31955157
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Prenatal and postnatal findings in small-for-gestational-age fetuses without structural ultrasound anomalies at 18-24 weeks.
    de Wit MC; Srebniak MI; Joosten M; Govaerts LC; Kornelisse RF; Papatsonis DN; de Graaff K; Knapen MF; Bruggenwirth HT; de Vries FA; Van Veen S; Van Opstal D; Galjaard RJ; Go AT
    Ultrasound Obstet Gynecol; 2017 Mar; 49(3):342-348. PubMed ID: 27102944
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Study on several ultrasound markers combined maternal serum biochemical markers to screen fetal chromosomal aneuploidy at 11 to 13(+)6 weeks of gestation].
    Chen X; Chang Y; Cui HY; Ren CC; Yu BY
    Zhonghua Fu Chan Ke Za Zhi; 2013 Nov; 48(11):815-8. PubMed ID: 24444556
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Fetal genetic findings by chromosomal microarray analysis and karyotyping for fetal growth restriction without structural malformations at a territory referral center: 10-year experience.
    Wu X; He S; Li Y; Guo D; Chen X; Liang B; Wang M; Huang H; Xu L
    BMC Pregnancy Childbirth; 2023 Jan; 23(1):73. PubMed ID: 36703098
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Fetal karyotyping after 28 weeks of gestation for late ultrasound findings in a low risk population.
    Drummond CL; Gomes DM; Senat MV; Audibert F; Dorion A; Ville Y
    Prenat Diagn; 2003 Dec; 23(13):1068-72. PubMed ID: 14691994
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Evaluation of routine prenatal ultrasound examination in detecting fetal chromosomal abnormalities in a low risk population.
    Stoll C; Dott B; Alembik Y; Roth MP
    Hum Genet; 1993 Mar; 91(1):37-41. PubMed ID: 8454285
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Application of chromosome microarray analysis in prenatal diagnosis.
    Xia M; Yang X; Fu J; Teng Z; Lv Y; Yu L
    BMC Pregnancy Childbirth; 2020 Nov; 20(1):696. PubMed ID: 33198662
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Ultrasound screening and diagnosis of fetal structural abnormalities between 11-14 gestational weeks].
    Markov D; Chernev T; Dimitrova V; Mazneĭkova V; Leroy Y; Jacquemyn Y; Ramaekers P; Van Bulck B; Loquet P
    Akush Ginekol (Sofiia); 2004; 43(3):3-10. PubMed ID: 15341249
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Next Generation Sequencing after Invasive Prenatal Testing in Fetuses with Congenital Malformations: Prenatal or Neonatal Investigation.
    Emms A; Castleman J; Allen S; Williams D; Kinning E; Kilby M
    Genes (Basel); 2022 Aug; 13(9):. PubMed ID: 36140685
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cytogenetic analysis in fetuses with late onset abnormal sonographic findings.
    Bardin R; Hadar E; Haizler-Cohen L; Gabbay-Benziv R; Meizner I; Kahana S; Yeshaya J; Yacobson S; Cohen-Vig L; Agmon-Fishman I; Basel-Vanagaite L; Maya I
    J Perinat Med; 2018 Nov; 46(9):975-982. PubMed ID: 28915119
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Society for Maternal-Fetal Medicine Consult Series #57: Evaluation and management of isolated soft ultrasound markers for aneuploidy in the second trimester: (Replaces Consults #10, Single umbilical artery, October 2010; #16, Isolated echogenic bowel diagnosed on second-trimester ultrasound, August 2011; #17, Evaluation and management of isolated renal pelviectasis on second-trimester ultrasound, December 2011; #25, Isolated fetal choroid plexus cysts, April 2013; #27, Isolated echogenic intracardiac focus, August 2013).
    ; Prabhu M; Kuller JA; Biggio JR
    Am J Obstet Gynecol; 2021 Oct; 225(4):B2-B15. PubMed ID: 34171388
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Ultrasonographic findings of fetal aneuploidies in the second trimester--our experiences.
    Papp C; Szigeti Z; Tóth-Pál E; Hajdú J; Joó JG; Papp Z
    Fetal Diagn Ther; 2008; 23(2):105-13. PubMed ID: 18033966
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.