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.
233 related articles for article (PubMed ID: 31566912)
1. Clinical value of genetic analysis in prenatal diagnosis of short femur. Liu J; Huang L; He Z; Lin S; Wang Y; Luo Y Mol Genet Genomic Med; 2019 Nov; 7(11):e978. PubMed ID: 31566912 [TBL] [Abstract][Full Text] [Related]
2. Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restriction. Zhu H; Lin S; Huang L; He Z; Huang X; Zhou Y; Fang Q; Luo Y Prenat Diagn; 2016 Jul; 36(7):686-92. PubMed ID: 27221052 [TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of genetic aberrations in fetuses with short femur detected by ultrasound: A prospective cohort study. Li Q; Zhang Z; Wang J; Zhang H; Zhu H; Lai Y; Liu S; Wang H; Hu T Prenat Diagn; 2021 Aug; 41(9):1153-1163. PubMed ID: 34185917 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. [Clinical analysis of 21 cases with short fetal femur in the third trimester]. Ren Y; You YQ; Zhou HH; Wang LX; Xu H; Li RB; Wang SJ; Xie XX; Meng YG; Lu YP Zhonghua Fu Chan Ke Za Zhi; 2017 Feb; 52(2):86-92. PubMed ID: 28253570 [No Abstract] [Full Text] [Related]
7. Diagnostic accuracy and value of chromosomal microarray analysis for chromosomal abnormalities in prenatal detection: A prospective clinical study. Huang H; Wang Y; Zhang M; Lin N; An G; He D; Chen M; Chen L; Xu L Medicine (Baltimore); 2021 May; 100(20):e25999. PubMed ID: 34011095 [TBL] [Abstract][Full Text] [Related]
8. Outcome of fetuses with short femur length detected at second-trimester anomaly scan: a national survey. Mathiesen JM; Aksglaede L; Skibsted L; Petersen OB; Tabor A; Ultrasound Obstet Gynecol; 2014 Aug; 44(2):160-5. PubMed ID: 24357398 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. [The value of combined use of chromosomal karyotyping and chromosome microarray analysis for prenatal diagnosis]. Rao H; Liu Y; Lu Q; Huang N; Zhou J Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Apr; 37(4):392-396. PubMed ID: 32219820 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
15. [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]
16. The clinical use of chromosomal microarray analysis in detection of fetal chromosomal rearrangements: a study from China Mainland. Wu Y; Wang Y; Tao J; Han X; Zhao X; Liu C; Gao L; Cheng W Eur J Obstet Gynecol Reprod Biol; 2017 May; 212():44-50. PubMed ID: 28340467 [TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of fetuses conceived by assisted reproductive technology by karyotyping and chromosomal microarray analysis. Guo H; Sheng R; Zhang X; Jin X; Gu W; Liu T; Dong H; Jia R PeerJ; 2023; 11():e14678. PubMed ID: 36684682 [TBL] [Abstract][Full Text] [Related]
18. [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]
19. [Clinical value of genome-wide chromosome microarray technique in diagnosis of fetal cerebral ventriculomegaly]. Peng YX; Qiu YW; Chang QX; Yu YH; Zhong M; Li KR Nan Fang Yi Ke Da Xue Xue Bao; 2018 Mar; 38(3):353-357. PubMed ID: 29643044 [TBL] [Abstract][Full Text] [Related]
20. Analysis of genetic testing in fetuses with congenital heart disease of single atria and/or single ventricle in a Chinese prenatal cohort. Li M; Ye B; Chen Y; Gao L; Wu Y; Cheng W BMC Pediatr; 2023 Nov; 23(1):577. PubMed ID: 37980516 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]