962 related articles for article (PubMed ID: 26833920)
1. 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]
2. [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]
3. [Application of chromosomal microarray analysis for fetuses with ventricular septal defects].
Deng Q; Fu F; Li R; Jing X; Lei T; Yang X; Pan M; Zhen L; Han J; Liao C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):699-704. PubMed ID: 28981937
[TBL] [Abstract][Full Text] [Related]
4. Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort study.
Wang Y; Cao L; Liang D; Meng L; Wu Y; Qiao F; Ji X; Luo C; Zhang J; Xu T; Yu B; Wang L; Wang T; Pan Q; Ma D; Hu P; Xu Z
Am J Obstet Gynecol; 2018 Feb; 218(2):244.e1-244.e17. PubMed ID: 29128521
[TBL] [Abstract][Full Text] [Related]
5. Clinical application of SNP array analysis in fetuses with ventricular septal defects and normal karyotypes.
Fu F; Deng Q; Lei TY; Li R; Jing XY; Yang X; Liao C
Arch Gynecol Obstet; 2017 Nov; 296(5):929-940. PubMed ID: 28905115
[TBL] [Abstract][Full Text] [Related]
6. Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease.
Yan Y; Wu Q; Zhang L; Wang X; Dan S; Deng D; Sun L; Yao L; Ma Y; Wang L
Ultrasound Obstet Gynecol; 2014 Apr; 43(4):404-12. PubMed ID: 24323407
[TBL] [Abstract][Full Text] [Related]
7. Clinical application of targeted next-generation sequencing in fetuses with congenital heart defect.
Hu P; Qiao F; Wang Y; Meng L; Ji X; Luo C; Xu T; Zhou R; Zhang J; Yu B; Wang L; Wang T; Pan Q; Ma D; Liang D; Xu Z
Ultrasound Obstet Gynecol; 2018 Aug; 52(2):205-211. PubMed ID: 29536580
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis.
Mademont-Soler I; Morales C; Soler A; Martínez-Crespo JM; Shen Y; Margarit E; Clusellas N; Obón M; Wu BL; Sánchez A
Ultrasound Obstet Gynecol; 2013 Apr; 41(4):375-82. PubMed ID: 23233332
[TBL] [Abstract][Full Text] [Related]
10. Genetic Testing and Pregnancy Outcome Analysis of 362 Fetuses with Congenital Heart Disease Identified by Prenatal Ultrasound.
Luo S; Meng D; Li Q; Hu X; Chen Y; He C; Xie B; She S; Li Y; Fu C
Arq Bras Cardiol; 2018 Oct; 111(4):571-577. PubMed ID: 30133550
[TBL] [Abstract][Full Text] [Related]
11. Clinical application of chromosomal microarray analysis for the prenatal diagnosis of chromosomal abnormalities and copy number variations in fetuses with congenital heart disease.
Xia Y; Yang Y; Huang S; Wu Y; Li P; Zhuang J
Prenat Diagn; 2018 May; 38(6):406-413. PubMed ID: 29573438
[TBL] [Abstract][Full Text] [Related]
12. [Combined G-banded karyotyping and multiplex ligation-dependent probe amplification for the detection of chromosomal abnormalities in fetuses with congenital heart defects].
Liu Y; Xie J; Geng Q; Xu Z; Wu W; Luo F; Li S; Wang Q; Chen W; Tan H; Zhang H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):1-5. PubMed ID: 28186583
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Chromosomal microarray analysis in fetuses with an isolated congenital heart defect: A retrospective, nationwide, multicenter study in France.
Hureaux M; Guterman S; Hervé B; Till M; Jaillard S; Redon S; Valduga M; Coutton C; Missirian C; Prieur F; Simon-Bouy B; Beneteau C; Kuentz P; Rooryck C; Gruchy N; Marle N; Plutino M; Tosca L; Dupont C; Puechberty J; Schluth-Bolard C; Salomon L; Sanlaville D; Malan V; Vialard F
Prenat Diagn; 2019 May; 39(6):464-470. PubMed ID: 30896039
[TBL] [Abstract][Full Text] [Related]
15. Cell-free DNA test for pathogenic copy number variations: A retrospective study.
Duan HL; Li J; Wang WJ; Cram DS; Liu W; Cao PX; Zhu XY; Hu YL
Taiwan J Obstet Gynecol; 2021 Nov; 60(6):1066-1071. PubMed ID: 34794739
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Prenatal diagnosis of fetal multicystic dysplastic kidney via high-resolution whole-genome array.
Fu F; Chen F; Li R; Zhang Y; Pan M; Li D; Liao C
Nephrol Dial Transplant; 2016 Oct; 31(10):1693-8. PubMed ID: 26932690
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
Wang J; Chen L; Zhou C; Wang L; Xie H; Xiao Y; Zhu H; Hu T; Zhang Z; Zhu Q; Liu Z; Liu S; Wang H; Xu M; Ren Z; Yu F; Cram DS; Liu H
Am J Obstet Gynecol; 2018 Sep; 219(3):287.e1-287.e18. PubMed ID: 29852155
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of genetic aberrations in fetuses with pulmonary stenosis in southern China: a retrospective analysis.
Cai M; Guo N; Fu M; Chen Y; Liang B; Que Y; Ji Q; Huang H; Xu L; Lin N
BMC Med Genomics; 2023 May; 16(1):119. PubMed ID: 37248535
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
