Liu S - Search Results

1

Pilot study of a novel multi-functional noninvasive prenatal test on fetus aneuploidy, copy number variation, and single-gene disorder screening.

Luo Y, Jia B, Yan K, Liu S, Song X, Chen M, Jin F, Du Y, Wang J, Hong Y, Cao S, Li D, Dong M. Luo Y, et al. Among authors: liu s. Mol Genet Genomic Med. 2019 Apr;7(4):e00597. doi: 10.1002/mgg3.597. Epub 2019 Feb 14. Mol Genet Genomic Med. 2019. PMID: 30767419 Free PMC article.

2

[Chorionic villus cell culture and karyotype analysis in 110 cases of early spontaneous abortion].

Xiong L, Liu J, Deng K, Liu SP, Jia B, Wu RF, Zhong M, Zeng R. Xiong L, et al. Nan Fang Yi Ke Da Xue Xue Bao. 2009 Jan;29(1):64-7. Nan Fang Yi Ke Da Xue Xue Bao. 2009. PMID: 19218115 Chinese.

3

[Clinical application of SYBR Green I real-time fluorescence quantitative PCR for diagnosis of common chromosome aneuploidy].

Liu LJ, Xiong L, Liu J, Deng K, Liu SP, Wu RF, Jia B, Song LL, Zhong M, Zeng R. Liu LJ, et al. Nan Fang Yi Ke Da Xue Xue Bao. 2010 Jan;30(1):11-5. Nan Fang Yi Ke Da Xue Xue Bao. 2010. PMID: 20117974 Chinese.

4

Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage.

Liu S, Song L, Cram DS, Xiong L, Wang K, Wu R, Liu J, Deng K, Jia B, Zhong M, Yang F. Liu S, et al. Among authors: liu j. Ultrasound Obstet Gynecol. 2015 Oct;46(4):472-7. doi: 10.1002/uog.14849. Ultrasound Obstet Gynecol. 2015. PMID: 25767059 Free article.

5

[Analysis of copy number variations in alpha-globin gene in the cases with combined increased levels of HbF with β thalassemia].

Liu S, Song L, Xiong L, Wang K, Shen H, Zhong M. Liu S, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Aug;32(4):515-9. doi: 10.3760/cma.j.issn.1003-9406.2015.04.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26252098 Chinese.

6

A novel contiguous deletion involving NDP, MAOB and EFHC2 gene in a patient with familial Norrie disease: bilateral blindness and leucocoria without other deficits.

Jia B, Huang L, Chen Y, Liu S, Chen C, Xiong K, Song L, Zhou Y, Yang X, Zhong M. Jia B, et al. Among authors: liu s. J Genet. 2017 Dec;96(6):1015-1020. doi: 10.1007/s12041-017-0869-5. J Genet. 2017. PMID: 29321361

7

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. Chang Q, et al. Among authors: liu s. Eur J Paediatr Neurol. 2020 Mar;25:106-112. doi: 10.1016/j.ejpn.2020.01.016. Epub 2020 Jan 22. Eur J Paediatr Neurol. 2020. PMID: 32014392

8

Prenatal Diagnosis of a Mosaic Paternal Uniparental Disomy for Chromosome 14: A Case Report of Kagami-Ogata Syndrome.

Li F, Liu S, Jia B, Wu R, Chang Q. Li F, et al. Among authors: liu s. Front Pediatr. 2021 Oct 21;9:691761. doi: 10.3389/fped.2021.691761. eCollection 2021. Front Pediatr. 2021. PMID: 34746047 Free PMC article.

9

A study on non-invasive prenatal screening for the detection of aneuploidy.

Chen Y, Yang F, Shang X, Liu S, Li M, Zhong M. Chen Y, et al. Among authors: liu s. Ginekol Pol. 2022;93(9):716-720. doi: 10.5603/GP.a2021.0254. Epub 2022 Mar 22. Ginekol Pol. 2022. PMID: 35315016 Free article.

10

Positive predictive value estimates for noninvasive prenatal testing from data of a prenatal diagnosis laboratory and literature review.

Liu S, Yang F, Chang Q, Jia B, Xu Y, Wu R, Li L, Chen W, Yin A, Huang F, Feng S, Li F. Liu S, et al. Mol Cytogenet. 2022 Jul 6;15(1):29. doi: 10.1186/s13039-022-00607-z. Mol Cytogenet. 2022. PMID: 35794576 Free PMC article.

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