Chen S - Search Results

1

Case report: A novel heterozygous synonymous variant in deep exon region of NIPBL gene generating a non-canonical splice donor in a patient with cornelia de lange syndrome.

Shi M, Liang Y, Xie B, Wei X, Zheng H, Gui C, Huang R, Fan X, Li C, Wei X, Ma Y, Chen S, Chen Y, Gui B. Shi M, et al. Among authors: chen s, chen y. Front Genet. 2022 Nov 23;13:1056127. doi: 10.3389/fgene.2022.1056127. eCollection 2022. Front Genet. 2022. PMID: 36506332 Free PMC article.

2

[Impact of gonadotropin-releasing hormone analogs treatment on final height in girls with central precocious puberty].

Chen SK, Fan X, Tang Q. Chen SK, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2009 May;11(5):374-6. Zhongguo Dang Dai Er Ke Za Zhi. 2009. PMID: 19470261 Chinese.

3

[Relationship between alanine aminotransferase and overweight or obesity in children].

Fan X, Chen SK, Tang Q, Luo JS, Feng Y. Fan X, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2011 Dec;13(12):951-4. Zhongguo Dang Dai Er Ke Za Zhi. 2011. PMID: 22172257 Free article. Chinese.

4

[Epidemiological study on the association between obesity with metabolic syndrome in obese children and adolescents of Nanning city, Guangxi].

Chen SK, Luo JS, Qin YF, Fan X, Tang Q, Feng Y. Chen SK, et al. Zhonghua Liu Xing Bing Xue Za Zhi. 2011 Oct;32(10):969-72. Zhonghua Liu Xing Bing Xue Za Zhi. 2011. PMID: 22333076 Chinese.

5

[Pulmonary surfactant associated gene variants in mixed ethnic population of Han and Zhuang].

Chen YJ, Chen SK, DePass K, Wegner DJ, Hamvas A, Nong GM, Wang YZ, Fan X, Luo JS. Chen YJ, et al. Zhonghua Er Ke Za Zhi. 2012 Nov;50(11):843-6. Zhonghua Er Ke Za Zhi. 2012. PMID: 23302616 Chinese.

6

[Prevalence of hypertension and relationship between hypertension and obesity in children and adolescents in Nanning of Guangxi Province].

Luo JS, Chen SK, Fan X, Tang Q, Feng Y. Luo JS, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2014 Oct;16(10):1040-4. Zhongguo Dang Dai Er Ke Za Zhi. 2014. PMID: 25344188 Free article. Chinese.

7

Mutation screening of the sodium iodide symporter gene in a cohort of 105 China patients with congenital hypothyroidism.

Fu C, Chen S, Chen R, Fan X, Luo J, Li C, Qian J. Fu C, et al. Among authors: chen r, chen s. Arq Bras Endocrinol Metabol. 2014 Nov;58(8):828-32. doi: 10.1590/0004-2730000003436. Epub 2014 Nov 1. Arq Bras Endocrinol Metabol. 2014. PMID: 25465605

8

[ASS1 gene mutation in a neonate with citrullinemia type I].

Xie B, Chen R, Wang J, Luo J, Li W, Chen S. Xie B, et al. Among authors: chen r, chen s. Zhonghua Er Ke Za Zhi. 2014 Oct;52(10):788-91. Zhonghua Er Ke Za Zhi. 2014. PMID: 25537548 Chinese.

9

Clinical and molecular evaluations of siblings with "pure" 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3).

Chen R, Li C, Xie B, Wang J, Fan X, Luo J, Hu X, Chen S, Shen Y. Chen R, et al. Among authors: chen s. Mol Cytogenet. 2014 Dec 24;7(1):101. doi: 10.1186/s13039-014-0101-8. eCollection 2014. Mol Cytogenet. 2014. PMID: 25648949 Free PMC article.

10

EPHA4 haploinsufficiency is responsible for the short stature of a patient with 2q35-q36.2 deletion and Waardenburg syndrome.

Li C, Chen R, Fan X, Luo J, Qian J, Wang J, Xie B, Shen Y, Chen S. Li C, et al. Among authors: chen r, chen s. BMC Med Genet. 2015 Apr 11;16:23. doi: 10.1186/s12881-015-0165-2. BMC Med Genet. 2015. PMID: 25928000 Free PMC article.

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