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.
3. The yield of chromosomal microarray in pregnancies with congenital cardiac defects and normal noninvasive prenatal screening. Sagi-Dain L; Singer A; Segel R; Berger R; Kanengisser-Pines B; Maya I Am J Obstet Gynecol; 2021 Sep; 225(3):333.e1-333.e14. PubMed ID: 34052193 [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. [Prenatal diagnosis and clinical outcomes of 297 fetuses with conotruncal defects]. Cao Q; Xu LL; Li R; Han J; Yi CX; Jing XY; Zhang LN; Li DZ; Pan M Zhonghua Fu Chan Ke Za Zhi; 2022 Jan; 57(1):25-31. PubMed ID: 35090242 [No Abstract] [Full Text] [Related]
6. 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]
7. Prevalence of chromosomal abnormalities and 22q11.2 deletion in conotruncal and non-conotruncal antenatally diagnosed congenital heart diseases in a Chinese population. Kong CW; Cheng YKY; To WWK; Leung TY Hong Kong Med J; 2019 Feb; 25(1):6-12. PubMed ID: 30655461 [TBL] [Abstract][Full Text] [Related]
8. Clinical value of chromosomal microarray analysis in prenatally diagnosed dextro-transposition of the great arteries. Lee MY; Won HS; Han YJ; Ryu HM; Lee DE; Jeong BD J Matern Fetal Neonatal Med; 2020 May; 33(9):1480-1485. PubMed ID: 30176760 [No Abstract] [Full Text] [Related]
9. 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]
10. Prenatal chromosomal microarray analysis in a large Chinese cohort of fetuses with congenital heart defects: a single center study. Lu Q; Luo L; Zeng B; Luo H; Wang X; Qiu L; Yang Y; Feng C; Zhou J; Hu Y; Huang T; Ma P; Huang T; Xie K; Yuan H; Huang S; Yang B; Zou Y; Liu Y Orphanet J Rare Dis; 2024 Aug; 19(1):307. PubMed ID: 39175064 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype. Wu X; Li Y; Su L; Xie X; Cai M; Lin N; Huang H; Lin Y; Xu L Mol Diagn Ther; 2020 Oct; 24(5):611-619. PubMed ID: 32651932 [TBL] [Abstract][Full Text] [Related]
14. Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis. Chau MHK; Cao Y; Kwok YKY; Chan S; Chan YM; Wang H; Yang Z; Wong HK; Leung TY; Choy KW Am J Obstet Gynecol; 2019 Nov; 221(5):493.e1-493.e11. PubMed ID: 31207233 [TBL] [Abstract][Full Text] [Related]
15. Genetic anomalies in fetuses with tetralogy of Fallot by using high-definition chromosomal microarray analysis. Peng R; Zheng J; Xie HN; He M; Lin MF Cardiovasc Ultrasound; 2019 May; 17(1):8. PubMed ID: 31060568 [TBL] [Abstract][Full Text] [Related]
16. The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings. Hui AS; Chau MHK; Chan YM; Cao Y; Kwan AH; Zhu X; Kwok YK; Chen Z; Lao TT; Choy KW; Leung TY Acta Obstet Gynecol Scand; 2021 Feb; 100(2):235-243. PubMed ID: 32981064 [TBL] [Abstract][Full Text] [Related]