Luo C - Search Results

1

Copy Number Variations with Isolated Fetal Ventriculomegaly.

Hu P, Wang Y, Sun R, Cao L, Chen X, Liu C, Luo C, Ma D, Wang W, Fu X, Shi W, Yi S, Zhang K, Liu H, Xu Z. Hu P, et al. Among authors: luo c. Curr Mol Med. 2017;17(2):133-139. doi: 10.2174/1566524017666170303125529. Curr Mol Med. 2017. PMID: 28260505

2

[Molecular and prenatal diagnosis for a Chinese pregnant woman with a novel mutation of β thalassemia].

Hao Y, Xu ZY, Jin Q, Wu WQ, Cai J, Luo CQ, Xie JS. Hao Y, et al. Zhonghua Xue Ye Xue Za Zhi. 2011 Apr;32(4):245-8. Zhonghua Xue Ye Xue Za Zhi. 2011. PMID: 21569707 Chinese.

3

[Analysis of copy number variations in an infant with Cri du Chat syndrome by array-based comparative genomic hybridization].

Luo FW, Luo CQ, Xie JS, Gen Q, Liu H, Li F, Chen WB, Wang L. Luo FW, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Aug;30(4):443-6. doi: 10.3760/cma.j.issn.1003-9406.2013.04.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23926013 Chinese.

4

Clinical application of SNP array analysis in first-trimester pregnancy loss: a prospective study.

Wang Y, Cheng Q, Meng L, Luo C, Hu H, Zhang J, Cheng J, Xu T, Jiang T, Liang D, Hu P, Xu Z. Wang Y, et al. Among authors: luo c. Clin Genet. 2017 Jun;91(6):849-858. doi: 10.1111/cge.12926. Epub 2016 Dec 22. Clin Genet. 2017. PMID: 27883173

5

[Genetic analysis and prenatal diagnosis for ten families affected with tuberous sclerosis complex].

Pan Y, Wu W, Luo C, Xie J, Xu Z, Geng Q, Hao Y. Pan Y, et al. Among authors: luo c. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Feb 10;35(1):18-22. doi: 10.3760/cma.j.issn.1003-9406.2018.01.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29419853 Chinese.

6

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. Hu P, et al. Among authors: luo c. Ultrasound Obstet Gynecol. 2018 Aug;52(2):205-211. doi: 10.1002/uog.19042. Epub 2018 Jun 25. Ultrasound Obstet Gynecol. 2018. PMID: 29536580 Free article.

7

Systematic analysis of copy-number variations associated with early pregnancy loss.

Wang Y, Li Y, Chen Y, Zhou R, Sang Z, Meng L, Tan J, Qiao F, Bao Q, Luo D, Peng C, Wang YS, Luo C, Hu P, Xu Z. Wang Y, et al. Among authors: luo c, luo d. Ultrasound Obstet Gynecol. 2020 Jan;55(1):96-104. doi: 10.1002/uog.20412. Ultrasound Obstet Gynecol. 2020. PMID: 31364215 Free article.

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. Qiao F, et al. Among authors: luo c. Ultrasound Obstet Gynecol. 2021 Sep;58(3):377-387. doi: 10.1002/uog.23532. Ultrasound Obstet Gynecol. 2021. PMID: 33142350 Free article.

9

[Clinical significance of large-scale screening of A1555G mutation of mitochondria DNA for neonates].

Cai J, Luo CQ, Xie JS, Wu WQ, Geng Q, Xu ZY, Hao Y, Xu XX. Cai J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Aug;28(4):414-6. doi: 10.3760/cma.j.issn.1003-9406.2011.04.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21811982 Chinese.

10

Application of Whole-Exome Sequencing in the Prenatal Diagnosis of Foetuses With Central Nervous System Abnormalities.

Luo C, Wen E, Liu Y, Wang H, Jia B, Chen L, Wu X, Geng Q, Wen H, Li S, Liu B, Wu W, Zhong M. Luo C, et al. Mol Genet Genomic Med. 2024 Oct;12(10):e70016. doi: 10.1002/mgg3.70016. Mol Genet Genomic Med. 2024. PMID: 39359128 Free PMC article.

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