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 *

199 related articles for article (PubMed ID: 24901266)

  • 41. Fetal ultrasound abnormalities: correlation with fetal karyotype, autopsy findings, and postnatal outcome--five-year prospective study.
    Wilson RD; Chitayat D; McGillivray BC
    Am J Med Genet; 1992 Nov; 44(5):586-90. PubMed ID: 1481814
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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]  

  • 43. Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive cases.
    Chong HP; Hamilton S; Mone F; Cheung KW; Togneri FS; Morris RK; Quinlan-Jones E; Williams D; Allen S; McMullan DJ; Kilby MD
    Prenat Diagn; 2019 Nov; 39(12):1064-1069. PubMed ID: 31393021
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 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]  

  • 45. The karyotype of fetuses with anomalies detected by second trimester ultrasonography.
    Gonen R; Dar H; Degani S
    Eur J Obstet Gynecol Reprod Biol; 1995 Feb; 58(2):153-5. PubMed ID: 7774742
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Association between fetal ventricular septal defects and chromosomal abnormalities].
    Du L; Xie HN; Li LJ; Zhu YX; Lin MF; Zheng J
    Zhonghua Fu Chan Ke Za Zhi; 2013 Nov; 48(11):805-9. PubMed ID: 24444554
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [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]  

  • 48. Clinical application of SNP array analysis in fetuses with ventricular septal defects and normal karyotypes.
    Fu F; Deng Q; Lei TY; Li R; Jing XY; Yang X; Liao C
    Arch Gynecol Obstet; 2017 Nov; 296(5):929-940. PubMed ID: 28905115
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Fetal right aortic arch: associated anomalies, genetic anomalies with chromosomal microarray analysis, and postnatal outcome.
    Peng R; Xie HN; Zheng J; Zhou Y; Lin MF
    Prenat Diagn; 2017 Apr; 37(4):329-335. PubMed ID: 28165153
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Fetal outcome in nuchal translucency with emphasis on normal fetal karyotype.
    Cha'ban FK; Van Splunder P; Los FJ; Wladimiroff JW
    Prenat Diagn; 1996 Jun; 16(6):537-41. PubMed ID: 8809895
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in fetuses with ultrasound anomalies in the urinary system.
    Hu T; Zhang Z; Wang J; Li Q; Zhu H; Lai Y; Wang H; Liu S
    Prenat Diagn; 2019 Nov; 39(12):1096-1106. PubMed ID: 31461547
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A correlative study of prenatal ultrasound and post-mortem findings in fetuses and infants with an abnormal karyotype.
    Isaksen CV; Eik-Nes SH; Blaas HG; Torp SH; van der Hagen CB; Ormerod E
    Ultrasound Obstet Gynecol; 2000 Jul; 16(1):37-45. PubMed ID: 11084963
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Incidence of chromosomal abnormalities in 153 pregnancies with ultrasound detected fetal abnormalities.
    Chew S; Anandakumar C; Jayanthi V; Wong YC; Chia D; Arulkumaran S; Ratnam SS
    Singapore Med J; 1996 Dec; 37(6):595-7. PubMed ID: 9104057
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature.
    de Wit MC; Srebniak MI; Govaerts LC; Van Opstal D; Galjaard RJ; Go AT
    Ultrasound Obstet Gynecol; 2014 Feb; 43(2):139-46. PubMed ID: 23897843
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Detection of copy number variants using chromosomal microarray analysis for the prenatal diagnosis of congenital heart defects with normal karyotype.
    Song T; Wan S; Li Y; Xu Y; Dang Y; Zheng Y; Li C; Zheng J; Chen B; Zhang J
    J Clin Lab Anal; 2019 Jan; 33(1):e22630. PubMed ID: 30047171
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Chromosomal microarray analysis and prenatal diagnosis.
    Lo JO; Shaffer BL; Feist CD; Caughey AB
    Obstet Gynecol Surv; 2014 Oct; 69(10):613-21. PubMed ID: 25336071
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Karyotyping of fetuses with developmental disorders. A 5-year material 1985-89].
    Tuveng JM; Eik-Nes SH; Sviggum O; Isaksen C; Berg K; Leren TP; van der Hagen CB
    Tidsskr Nor Laegeforen; 1993 Jan; 113(3):339-42. PubMed ID: 8441983
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Role of magnetic resonance imaging in fetuses with mild or moderate ventriculomegaly in the era of fetal neurosonography: systematic review and meta-analysis.
    Di Mascio D; Sileo FG; Khalil A; Rizzo G; Persico N; Brunelli R; Giancotti A; Panici PB; Acharya G; D'Antonio F
    Ultrasound Obstet Gynecol; 2019 Aug; 54(2):164-171. PubMed ID: 30549340
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Ultrasonographically detectable markers of fetal chromosomal abnormalities.
    Nicolaides KH; Snijders RJ; Gosden CM; Berry C; Campbell S
    Lancet; 1992 Sep; 340(8821):704-7. PubMed ID: 1355807
    [TBL] [Abstract][Full Text] [Related]  

  • 60. First-trimester screening for trisomies 18 and 13, triploidy and Turner syndrome by detailed early anomaly scan.
    Wagner P; Sonek J; Hoopmann M; Abele H; Kagan KO
    Ultrasound Obstet Gynecol; 2016 Oct; 48(4):446-451. PubMed ID: 26611869
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.