BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 36703098)

  • 1. 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]  

  • 2. Etiologic evaluation and pregnancy outcomes of fetal growth restriction (FGR) associated with structural malformations.
    Wu X; He S; Shen Q; Xu S; Guo D; Liang B; Wang X; Cao H; Huang H; Xu L
    Sci Rep; 2024 Apr; 14(1):9220. PubMed ID: 38649697
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. The genetics and clinical outcomes in 151 cases of fetal growth restriction: A Chinese single-center study.
    Peng C; Hu L; Bu X; Li H; Jiang X; Zhou S; Deng L; He J; LinPeng S
    Eur J Obstet Gynecol Reprod Biol; 2024 Jul; 298():128-134. PubMed ID: 38756052
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis.
    Xie X; Huang B; Su L; Cai M; Chen Y; Wu X; Xu L
    BMC Med Genomics; 2023 Nov; 16(1):298. PubMed ID: 37986075
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restriction.
    Zhu H; Lin S; Huang L; He Z; Huang X; Zhou Y; Fang Q; Luo Y
    Prenat Diagn; 2016 Jul; 36(7):686-92. PubMed ID: 27221052
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center.
    Cai M; Lin N; Su L; Wu X; Xie X; Xu S; Fu X; Xu L; Huang H
    J Transl Med; 2022 Apr; 20(1):168. PubMed ID: 35397568
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of non-mosaic sex chromosome abnormalities: a 10-year experience from a tertiary referral center.
    Wu X; Guo D; Li Y; Xie X; Su L; Cai M; Zheng L; Lin N; Liang B; Huang H; Xu L
    J Perinat Med; 2023 Sep; 51(7):904-912. PubMed ID: 37138453
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. Single nucleotide polymorphism array (SNP-array) analysis for fetuses with abnormal nasal bone.
    Xie X; Su L; Li Y; Shen Q; Wang M; Wu X
    Arch Gynecol Obstet; 2024 Jun; 309(6):2475-2482. PubMed ID: 37430178
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Should prenatal chromosomal microarray analysis be offered for isolated fetal growth restriction? A French multicenter study.
    Monier I; Receveur A; Houfflin-Debarge V; Goua V; Castaigne V; Jouannic JM; Mousty E; Saliou AH; Bouchghoul H; Rousseau T; Valat AS; Groussolles M; Fuchs F; Benoist G; Degre S; Massardier J; Tsatsaris V; Kleinfinger P; Zeitlin J; Benachi A;
    Am J Obstet Gynecol; 2021 Dec; 225(6):676.e1-676.e15. PubMed ID: 34058167
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Clinical features of abnormal chromosome karyotypes in twin pregnancies complicated with structural abnormalities].
    Zhong SL; Fang Q; Chen BJ; Han ZY; Luo YM; Chen JS; Xie YJ
    Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):649-54. PubMed ID: 22176987
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Second trimester growth restriction and underlying fetal anomalies].
    Vanlieferinghen S; Bernard JP; Salomon LJ; Chalouhi GE; Russell NE; Ville Y
    Gynecol Obstet Fertil; 2014 Sep; 42(9):567-71. PubMed ID: 25164160
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomalies.
    Beulen L; Faas BHW; Feenstra I; van Vugt JMG; Bekker MN
    Ultrasound Obstet Gynecol; 2017 Jun; 49(6):721-728. PubMed ID: 27515011
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prenatal screening for fetal aneuploidy in singleton pregnancies.
    Chitayat D; Langlois S; Douglas Wilson R; ;
    J Obstet Gynaecol Can; 2011 Jul; 33(7):736-750. PubMed ID: 21749752
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Incidence, clinical features and perinatal outcome in anomalous fetuses with late-onset growth restriction: cohort study.
    Dall'Asta A; Stampalija T; Mecacci F; Ramirez Zegarra R; Sorrentino S; Minopoli M; Ottaviani C; Fantasia I; Barbieri M; Lisi F; Simeone S; Castellani R; Fichera A; Rizzo G; Prefumo F; Frusca T; Ghi T
    Ultrasound Obstet Gynecol; 2022 Nov; 60(5):632-639. PubMed ID: 35638182
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The Yield of Chromosomal Microarray in Pregnancies Complicated with Fetal Growth Restriction Can Be Predicted According to Clinical Parameters.
    Tzadikevitch Geffen K; Singer A; Maya I; Ben-Shachar S; Sagi-Dain L; Daum H; Michaelson-Cohen R; Greenbaum L; Feingold-Zadok M; Sukenik Halevy R
    Fetal Diagn Ther; 2021; 48(2):140-148. PubMed ID: 33352557
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Prenatal diagnosis of women with an adverse reproductive history using both traditional karyotyping and SNP-array].
    Yu HS; Guo H; Shen SS; Li XC; Zhang LP; Fan XF
    Zhonghua Fu Chan Ke Za Zhi; 2018 Mar; 53(3):155-159. PubMed ID: 29609228
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.