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 *

154 related articles for article (PubMed ID: 37430178)

  • 1. 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]  

  • 2. [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]  

  • 3. Assessing the value of second-trimester nasal bone hypoplasia in predicting chromosomal abnormalities: a retrospective chromosomal microarray analysis of 351 fetuses.
    Pan L; Liang H; Meng Z; Wang J; Zhang R; Wu Y
    Arch Gynecol Obstet; 2023 Oct; 308(4):1263-1270. PubMed ID: 36269386
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markers.
    Cai M; Lin N; Chen X; Fu M; Guo N; Xu L; Huang H
    BMC Med Genomics; 2021 Jan; 14(1):19. PubMed ID: 33435955
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hypoplastic nasal bone: A potential marker for facial dysmorphism associated with pathogenic copy number variants on microarray.
    Gu YZ; Nisbet DL; Reidy KL; Palma-Dias R
    Prenat Diagn; 2019 Jan; 39(2):116-123. PubMed ID: 30578730
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. [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]  

  • 9. Prenatal chromosomal microarray analysis in 2466 fetuses with ultrasonographic soft markers: a prospective cohort study.
    Hu T; Tian T; Zhang Z; Wang J; Hu R; Xiao L; Zhu H; Lai Y; Wang H; Liu S
    Am J Obstet Gynecol; 2021 May; 224(5):516.e1-516.e16. PubMed ID: 33122027
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic evaluation for twin pregnancies using karyotyping and single nucleotide polymorphism array analysis.
    Wu X; Huang B; Xie X; Cai M; Chen Y; Liang B; Shen Q; Guo D; Lin N; Su L; Xu L
    Gene; 2024 Feb; 895():148005. PubMed ID: 37977315
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromosomal Microarray Analysis for the Prenatal Diagnosis in Fetuses with Nasal Bone Hypoplasia: A Retrospective Cohort Study.
    Huang H; Cai M; Ma W; Lin N; Xu L
    Risk Manag Healthc Policy; 2021; 14():1533-1540. PubMed ID: 33889037
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Is Noninvasive Prenatal Screening Appropriate for Pregnant Women Age 35 or Older In Cases if Isolated Fetal Nasal Bone Abnormalities in The Chinese Han Population?
    Chen Y; Lv M; Dong T; Chen Q; Qian Y; Zhao B; Luo Q
    Med Sci Monit; 2020 Jul; 26():e924387. PubMed ID: 32712620
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Single nucleotide polymorphism microarray in prenatal diagnosis of fetuses with absent nasal bone].
    Yu J; Sun Y; Hu J; Qian Y; Luo Y; Dong M
    Zhejiang Da Xue Xue Bao Yi Xue Ban; 2019 Jun; 48(4):414-419. PubMed ID: 31901046
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Application of chromosomal analysis for 29 cases of fetuses with nasal bone absence or hypoplasia].
    Hou L; Wang XX; Jiang HL; Zhang T; Li L; Zhang WY; Wang X
    Zhonghua Yi Xue Za Zhi; 2018 Nov; 98(43):3532-3535. PubMed ID: 30481905
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Detection of copy number variants with chromosomal microarray in 10 377 pregnancies at a single laboratory.
    Lin YH; Jong YJ; Huang PC; Tsai C
    Acta Obstet Gynecol Scand; 2020 Jun; 99(6):775-782. PubMed ID: 32346853
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Advanced maternal age: copy number variations and pregnancy outcomes.
    Cao L; Dong W; Wu Q; Huang X; Zeng X; Yang J; Lu J; Chen X; Zheng X; Fu X
    Front Genet; 2023; 14():1206855. PubMed ID: 37396033
    [No Abstract]   [Full Text] [Related]  

  • 20. Maternal serum biochemistry at 11-13(+6) weeks in relation to the presence or absence of the fetal nasal bone on ultrasonography in chromosomally abnormal fetuses: an updated analysis of integrated ultrasound and biochemical screening.
    Cicero S; Spencer K; Avgidou K; Faiola S; Nicolaides KH
    Prenat Diagn; 2005 Nov; 25(11):977-83. PubMed ID: 16245371
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.