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 *

148 related articles for article (PubMed ID: 35506821)

  • 1. Prenatal chromosomal microarray analysis in foetuses with isolated absent or hypoplastic nasal bone.
    Shi X; Lu J; Li L; Wei R; Wu J
    Ann Med; 2022 Dec; 54(1):1297-1302. PubMed ID: 35506821
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. First-trimester absent nasal bone: is it a predictive factor for pathogenic CNVs in the low-risk population?
    Fantasia I; Stampalija T; Sirchia F; Della Pietà I; Ottaviani Giammarco C; Guidolin F; Quadrifoglio M; Barresi V; Travan L; Faletra F
    Prenat Diagn; 2020 Dec; 40(12):1563-1568. PubMed ID: 32799336
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Estimating the frequency of causal genetic variants in foetuses with congenital heart defects: a Chinese cohort study.
    Lu F; Xue P; Zhang B; Wang J; Yu B; Liu J
    Orphanet J Rare Dis; 2022 Jan; 17(1):2. PubMed ID: 34983622
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. First-trimester assessment of nasal bone using retronasal triangle view: a prospective study.
    Adiego B; Martinez-Ten P; Illescas T; Bermejo C; Sepulveda W
    Ultrasound Obstet Gynecol; 2014 Mar; 43(3):272-6. PubMed ID: 23733531
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in foetuses with ventriculomegaly.
    Wang J; Zhang Z; Li Q; Zhu H; Lai Y; Luo W; Liu S; Wang H; Hu T
    Sci Rep; 2020 Nov; 10(1):20765. PubMed ID: 33247184
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. [Prenatal genetic diagnosis of the fetuses with isolated corpus callosum abnormality].
    She Q; Zhen L; Fu F; Lei TY; Li LS; Li R; Wang D; Zhang YL; Jing XY; Yi CX; Zhong HZ; Tan WH; Li FG; Liao C
    Zhonghua Fu Chan Ke Za Zhi; 2022 Sep; 57(9):671-677. PubMed ID: 36177578
    [No Abstract]   [Full Text] [Related]  

  • 13. [Application of chromosomal microarray analysis in prenatal diagnosis of pregnant women with advanced age].
    Yang S; Zhao Y; Tang X; Wang Z; Liu D; Zhang J; Gu Y; Wang L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Feb; 38(2):101-107. PubMed ID: 33565058
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Isolated absent or hypoplastic nasal bone in the second trimester fetus: is amniocentesis necessary?
    Ting YH; Lao TT; Lau TK; Chung MK; Leung TY
    J Matern Fetal Neonatal Med; 2011 Apr; 24(4):555-8. PubMed ID: 21375370
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. [Analysis of copy number variation by CMA in fetus with increased nuchal translucency].
    Du L; Xie HN; Zheng J; He M
    Zhonghua Fu Chan Ke Za Zhi; 2018 Oct; 53(10):671-676. PubMed ID: 30369122
    [No Abstract]   [Full Text] [Related]  

  • 19. Normal Range of Fetal Nasal Bone Length during the Second Trimester in an Afro-Caribbean Population and Likelihood Ratio for Trisomy 21 of Absent or Hypoplastic Nasal Bone.
    Gautier M; Gueneret M; Plavonil C; Jolivet E; Schaub B
    Fetal Diagn Ther; 2017; 42(2):130-136. PubMed ID: 27764826
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of tissue from pregnancy loss and aborted fetus with ultrasound anomaly using subtelomeric MLPA and chromosomal array analysis.
    Lou J; Sun M; Zhao Y; Fu Y; Yuan H; Dai Y; Liang F; He Y; Liu Y
    J Matern Fetal Neonatal Med; 2022 Aug; 35(16):3064-3069. PubMed ID: 32811234
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.