Liu S - Search Results

1

Clinical Application of an Innovative Multiplex-Fluorescent-Labeled STRs Assay for Prader-Willi Syndrome and Angelman Syndrome.

Zhang K, Liu S, Feng B, Yang Y, Zhang H, Dong R, Liu Y, Gai Z. Zhang K, et al. Among authors: liu y, liu s. PLoS One. 2016 Feb 3;11(2):e0147824. doi: 10.1371/journal.pone.0147824. eCollection 2016. PLoS One. 2016. PMID: 26841067 Free PMC article.

2

Uniparental Disomy of Chromosome 15 in Two Cases by Chromosome Microarray: A Lesson Worth Thinking.

Liu S, Zhang K, Song F, Yang Y, Lv Y, Gao M, Liu Y, Gai Z. Liu S, et al. Among authors: liu y. Cytogenet Genome Res. 2017;152(1):1-8. doi: 10.1159/000477520. Epub 2017 Jun 24. Cytogenet Genome Res. 2017. PMID: 28647735

3

Transmission of a Novel Imprinting Center Deletion Associated With Prader-Willi Syndrome Through Three Generations of a Chinese Family: Case Presentation, Differential Diagnosis, and a Lesson Worth Thinking About.

Zhang K, Liu S, Gu W, Lv Y, Yu H, Gao M, Wang D, Zhao J, Li X, Gai Z, Zhao S, Liu Y, Yuan Y. Zhang K, et al. Among authors: liu y, liu s. Front Genet. 2021 Aug 24;12:630650. doi: 10.3389/fgene.2021.630650. eCollection 2021. Front Genet. 2021. PMID: 34504512 Free PMC article.

4

Possibility of early diagnosis in a fetus affected by Prader‑Willi syndrome with maternal hetero‑UPD15: A lesson to be learned.

Dong Y, Liu S, Li J, Li J, Chen Q, Luo J, Li C, Li H, Qi H, Li R. Dong Y, et al. Among authors: liu s. Mol Med Rep. 2019 Jul;20(1):95-102. doi: 10.3892/mmr.2019.10246. Epub 2019 May 15. Mol Med Rep. 2019. PMID: 31115529 Free PMC article.

5

Prenatal diagnosis in a hereditary Peutz-Jeghers syndrome family with high cancer risk.

Wang Z, Liu S, Liu S, Wang Y, Chen J, Wu B. Wang Z, et al. Among authors: liu s. BMC Med Genet. 2018 May 2;19(1):66. doi: 10.1186/s12881-018-0594-9. BMC Med Genet. 2018. PMID: 29720104 Free PMC article.

6

Gray Matter Heterotopia, Mental Retardation, Developmental Delay, Microcephaly, and Facial Dysmorphisms in a Boy with Ring Chromosome 6: A 10-Year Follow-Up and Literature Review.

Liu S, Wang Z, Wei S, Liang J, Chen N, OuYang H, Zeng W, Chen L, Xie X, Jiang J. Liu S, et al. Cytogenet Genome Res. 2018;154(4):201-208. doi: 10.1159/000488692. Epub 2018 Apr 14. Cytogenet Genome Res. 2018. PMID: 29656294 Review.

7

Two novel STK11 missense mutations induce phosphorylation of S6K and promote cell proliferation in Peutz-Jeghers syndrome.

Li R, Wang Z, Liu S, Wu B, Zeng D, Zhang Y, Gong L, Deng F, Zheng H, Wang Y, Chen C, Chen J, Jiang B. Li R, et al. Among authors: liu s. Oncol Lett. 2018 Jan;15(1):717-726. doi: 10.3892/ol.2017.7436. Epub 2017 Nov 17. Oncol Lett. 2018. PMID: 29399144 Free PMC article.

8

Severe forms of complete androgen insensitivity syndrome caused by a p.Q65X novel mutation in androgen receptor: Clinical manifestations, imaging findings and molecular genetics.

Liu S, Wang Z, Jiang J, OuYang H, Wei S, Liang J, Chen N, Zeng W, Chen L, Xie X. Liu S, et al. Steroids. 2019 Apr;144:47-51. doi: 10.1016/j.steroids.2019.02.007. Epub 2019 Feb 8. Steroids. 2019. PMID: 30742848

9

Two novel mutations in the glycine decarboxylase gene in a boy with classic nonketotic hyperglycinemia: case report.

Liu S, Wang Z, Liang J, Chen N, OuYang H, Zeng W, Chen L, Xie X, Jiang J. Liu S, et al. Arch Argent Pediatr. 2017 Aug 1;115(4):e225-e229. doi: 10.5546/aap.2017.eng.e225. Arch Argent Pediatr. 2017. PMID: 28737873 Free article. English, Spanish.

10

Case Report: Successful Management of a 29-Day-Old Infant With Severe Hyperlipidemia From a Novel Homozygous Variant of GPIHBP1 Gene.

Liu S, Wang Z, Zheng X, Zhang Y, Wei S, OuYang H, Liang J, Chen N, Zeng W, Jiang J. Liu S, et al. Front Pediatr. 2022 Mar 10;10:792574. doi: 10.3389/fped.2022.792574. eCollection 2022. Front Pediatr. 2022. PMID: 35359903 Free PMC article.

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