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 *

274 related articles for article (PubMed ID: 35478332)

  • 1. Genetic diagnosis of common fetal renal abnormalities detected on prenatal ultrasound.
    Liu L; Li J; Li Y; Li H; Yang B; Fan H; Wang J; Gu Y; Yu H; Bai M; Yu T; Cui S; Cheng G; Ren C
    Prenat Diagn; 2022 Jun; 42(7):894-900. PubMed ID: 35478332
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China.
    Zhou Y; Lu X; Zhang Y; Ge Y; Xu Y; Wu L; Jiang Y
    Cytogenet Genome Res; 2022; 162(7):354-364. PubMed ID: 36907182
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis and outcomes in fetuses with duplex kidney.
    Ma C; Huang R; Fu F; Zhou H; Wang Y; Yan S; Guo F; Chen H; Li L; Jing X; Li F; Han J; Li D; Li R; Liao C
    Int J Gynaecol Obstet; 2024 Jul; 166(1):353-359. PubMed ID: 38189110
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 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. Whole exome sequencing as a diagnostic adjunct to clinical testing in fetuses with structural abnormalities.
    Fu F; Li R; Li Y; Nie ZQ; Lei T; Wang D; Yang X; Han J; Pan M; Zhen L; Ou Y; Li J; Li FT; Jing X; Li D; Liao C
    Ultrasound Obstet Gynecol; 2018 Apr; 51(4):493-502. PubMed ID: 28976722
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Prenatal diagnosis of polycystic renal diseases: diagnostic yield, novel disease-causing variants, and genotype-phenotype correlations.
    Huang R; Fu F; Guo F; Zhou H; Yu Q; Yan S; Liu L; Lu J; Ma C; Wang Y; Chen H; Wang D; Zhang Y; Jing X; Li F; Han J; Li D; Li R; Liao C
    Am J Obstet Gynecol MFM; 2024 Jan; 6(1):101228. PubMed ID: 37984685
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 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. 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]  

  • 14. Association of prenatal thoracic ultrasound abnormalities with copy number variants at a single Chinese tertiary center.
    Huang Q; Zhang Y; Jing X; Li F; Qin J; Li F; Li D; Li R; Liao C
    Int J Gynaecol Obstet; 2024 Feb; 164(2):770-777. PubMed ID: 37565521
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes.
    Qi Q; Jiang Y; Zhou X; Meng H; Hao N; Chang J; Bai J; Wang C; Wang M; Guo J; Ouyang Y; Xu Z; Xiao M; Zhang VW; Liu J
    Genes (Basel); 2020 Nov; 11(12):. PubMed ID: 33255631
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Application value of chromosome microarray analysis for prenatal diagnosis of fetus with ultrasonic abnormalities].
    Mi X; Shen X; Zhang S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jan; 37(1):67-70. PubMed ID: 31922601
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Copy number variations in multicystic dysplastic kidney: update for prenatal diagnosis and genetic counseling.
    Xi Q; Zhu X; Wang Y; Ru T; Dai C; Wang Z; Li J; Hu Y
    Prenat Diagn; 2016 May; 36(5):463-8. PubMed ID: 26941192
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis and pregnancy outcomes of fetuses with polyhydramnios.
    Liu Y; Hu T; Qian Y; Wang J; Hu R; Xiao L; Liao N; Liu Z; Wang H; Liu S; Zhang Z
    J Matern Fetal Neonatal Med; 2024 Dec; 37(1):2344089. PubMed ID: 38710614
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Molecular diagnostic in fetuses with isolated congenital anomalies of the kidney and urinary tract by whole-exome sequencing.
    Zhou X; Wang Y; Shao B; Wang C; Hu P; Qiao F; Xu Z
    J Clin Lab Anal; 2020 Nov; 34(11):e23480. PubMed ID: 32779812
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.