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 *

618 related articles for article (PubMed ID: 33142350)

  • 1. Comprehensive evaluation of genetic variants using chromosomal microarray analysis and exome sequencing in fetuses with congenital heart defect.
    Qiao F; Wang Y; Zhang C; Zhou R; Wu Y; Wang C; Meng L; Mao P; Cheng Q; Luo C; Hu P; Xu Z
    Ultrasound Obstet Gynecol; 2021 Sep; 58(3):377-387. PubMed ID: 33142350
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis for fetuses with isolated and non-isolated congenital heart defects using chromosomal microarray and exome sequencing.
    Xing Y; Zhang Y; Chen J; Wu F; Yuan M; Zou G; Yang Y; Zhou F; Zhou J; Sun L
    Prenat Diagn; 2022 Jun; 42(7):873-880. PubMed ID: 35584285
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exome sequencing as first-tier test for fetuses with severe central nervous system structural anomalies.
    Yaron Y; Ofen Glassner V; Mory A; Zunz Henig N; Kurolap A; Bar Shira A; Brabbing Goldstein D; Marom D; Ben Sira L; Baris Feldman H; Malinger G; Krajden Haratz K; Reches A
    Ultrasound Obstet Gynecol; 2022 Jul; 60(1):59-67. PubMed ID: 35229910
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Clinical value of genome-wide high resolution chromosomal microarray analysis in etiological study of fetuses with congenital heart defects].
    Wu X; Fu F; Li R; Pan M; Han J; Zhen L; Yang X; Zhang Y; Li F; Liao C
    Zhonghua Fu Chan Ke Za Zhi; 2014 Dec; 49(12):893-8. PubMed ID: 25608988
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal exome sequencing analysis in fetuses with central nervous system anomalies.
    Zhi Y; Liu L; Wang H; Chen X; Lv Y; Cui X; Chang H; Wang Y; Cui S
    Ultrasound Obstet Gynecol; 2023 Nov; 62(5):721-726. PubMed ID: 37204857
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing.
    Zhu X; Li J; Ru T; Wang Y; Xu Y; Yang Y; Wu X; Cram DS; Hu Y
    Prenat Diagn; 2016 Apr; 36(4):321-7. PubMed ID: 26833920
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Whole exome sequencing analysis of 37 fetuses with cardiac abnormalities].
    Xu X; Ye F; Zhang J; Jin K; Shen Q; Shen S; Jin F
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Aug; 41(8):903-908. PubMed ID: 39097270
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. The prevalence of genetic diagnoses in fetuses with severe congenital heart defects.
    van Nisselrooij AEL; Lugthart MA; Clur SA; Linskens IH; Pajkrt E; Rammeloo LA; Rozendaal L; Blom NA; van Lith JMM; Knegt AC; Hoffer MJV; Aten E; Santen GWE; Haak MC
    Genet Med; 2020 Jul; 22(7):1206-1214. PubMed ID: 32341573
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association of prenatal renal ultrasound abnormalities with pathogenic copy number variants in a large Chinese cohort.
    Su J; Qin Z; Fu H; Luo J; Huang Y; Huang P; Zhang S; Liu T; Lu W; Li W; Jiang T; Wei S; Yang S; Shen Y
    Ultrasound Obstet Gynecol; 2022 Feb; 59(2):226-233. PubMed ID: 34090309
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pregnancy outcomes of fetuses with congenital heart disease after a prenatal diagnosis with chromosome microarray.
    Zhang Z; Hu T; Wang J; Hu R; Li Q; Xiao L; Liao N; Liu Z; Wang H; Liu S
    Prenat Diagn; 2022 Jan; 42(1):79-86. PubMed ID: 34918366
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Yield rate of chromosomal microarray analysis in fetuses with congenital heart defects.
    Turan S; Asoglu MR; Gabbay-Benziv R; Doyle L; Harman C; Turan OM
    Eur J Obstet Gynecol Reprod Biol; 2018 Feb; 221():172-176. PubMed ID: 29306563
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital heart defects and copy number variants associated with neurodevelopmental impairment.
    Findley TO; Crain AK; Mahajan S; Deniwar A; Davis J; Solis Zavala AS; Corno AF; Rodriguez-Buritica D
    Am J Med Genet A; 2022 Jan; 188(1):13-23. PubMed ID: 34472185
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencing.
    Huang R; Fu F; Zhou H; Zhang L; Lei T; Cheng K; Yan S; Guo F; Wang Y; Ma C; Li R; Yu Q; Deng Q; Li L; Yang X; Han J; Li D; Liao C
    Hum Genet; 2023 Jun; 142(6):835-847. PubMed ID: 37095353
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic aetiology distribution of 398 foetuses with congenital heart disease in the prenatal setting.
    Yi T; Hao X; Sun H; Zhang Y; Han J; Gu X; Sun L; Liu X; Zhao Y; Guo Y; Zhou X; He Y
    ESC Heart Fail; 2023 Apr; 10(2):917-930. PubMed ID: 36478645
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The yield of SNP microarray analysis for fetal ultrasound cardiac abnormalities.
    Ye F; Xu X; Wang Y; Chen L; Shan Q; Wang Q; Jin F
    BMC Pregnancy Childbirth; 2024 Apr; 24(1):244. PubMed ID: 38580914
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Chromosomal abnormalities in fetuses with congenital heart disease: a meta-analysis.
    Wang H; Lin X; Lyu G; He S; Dong B; Yang Y
    Arch Gynecol Obstet; 2023 Sep; 308(3):797-811. PubMed ID: 36609702
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Diagnostic yield of whole exome data in fetuses aborted for conotruncal malformations.
    Shi JW; Cao H; Hong L; Ma J; Cui L; Zhang Y; Song X; Liu J; Yang Y; Lv Q; Zhang L; Wang J; Xie M
    Prenat Diagn; 2022 Jun; 42(7):852-861. PubMed ID: 35420166
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes.
    Al-Hamed MH; Kurdi W; Khan R; Tulbah M; AlNemer M; AlSahan N; AlMugbel M; Rafiullah R; Assoum M; Monies D; Shah Z; Rahbeeni Z; Derar N; Hakami F; Almutairi G; AlOtaibi A; Ali W; AlShammasi A; AlMubarak W; AlDawoud S; AlAmri S; Saeed B; Bukhari H; Ali M; Akili R; Alquayt L; Hagos S; Elbardisy H; Akilan A; Almuhana N; AlKhalifah A; Abouelhoda M; Ramzan K; Sayer JA; Imtiaz F
    Hum Genet; 2022 Jan; 141(1):101-126. PubMed ID: 34853893
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 31.