Mei S - Search Results

1

[Genetic analysis of a patient featuring developmental delay and mental retardation].

Bai N, Liu Y, Mei S, Kong X. Bai N, et al. Among authors: mei s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Apr;33(2):208-11. doi: 10.3760/cma.j.issn.1003-9406.2016.02.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27060317 Chinese.

2

[SNP array and cytogenetic analysis of a patient with unexplained mental retardation].

Bai N, Mei S, Zhao Z, Kong X. Bai N, et al. Among authors: mei s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Jun;33(3):332-4. doi: 10.3760/cma.j.issn.1003-9406.2016.03.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27264815 Chinese.

3

[Genetic analysis for a family affected with hemophilia type A due to a large deletion of F8 gene].

Bai N, Mei S, Liu N, Zhao Z, Meng J, Kong X. Bai N, et al. Among authors: mei s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Dec 10;33(6):782-785. doi: 10.3760/cma.j.issn.1003-9406.2016.06.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27984605 Chinese.

4

[Analysis of IDS gene mutation in a family affected with mucopolysaccharidosis typeⅡ].

Li Y, Mei S, Kong X, Zhao Z, Zhu X, Yang X, Qin Z, Wu H. Li Y, et al. Among authors: mei s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Feb 10;34(1):58-60. doi: 10.3760/cma.j.issn.1003-9406.2017.01.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28186595 Chinese.

5

[IDUA gene mutation analysis and prenatal diagnosis of two families affected with mucopolysaccharidosis type I].

Yang X, Mei S, Kong X, Zhao Z, Cai A, Yao J, Li Y, Qin Z. Yang X, et al. Among authors: mei s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Jun 10;34(3):347-351. doi: 10.3760/cma.j.issn.1003-9406.2017.03.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28604952 Chinese.

6

[Analysis of POMT1 gene mutation in a pedigree affected with congenital muscular dystrophy].

Chen C, Mei S, Zhu C, Ren Y, Kong X. Chen C, et al. Among authors: mei s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Feb 10;35(1):78-80. doi: 10.3760/cma.j.issn.1003-9406.2018.01.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29419866 Chinese.

7

[Genetic and prenatal diagnosis of a retinitis pigmentosa pedigree].

Kang H, Bai N, Mei S, Kong X. Kang H, et al. Among authors: mei s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Apr 10;35(2):184-187. doi: 10.3760/cma.j.issn.1003-9406.2018.02.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29652988 Chinese.

8

Identification of 4 novel mutations of androgen receptor gene in 8 Chinese families with complete androgen insensitivity syndrome.

Wu Q, Wang C, Shi H, Mei S, Liu L, Xin Y, Kong X. Wu Q, et al. Among authors: mei s. Clin Genet. 2018 Aug;94(2):269-270. doi: 10.1111/cge.13248. Epub 2018 Apr 25. Clin Genet. 2018. PMID: 29693241 No abstract available.

9

[Analysis of MUT gene mutations and prenatal diagnosis for 20 pedigrees affected with isolated methylmalonic aciduria].

Hu S, Mei S, Bai Y, Kong X. Hu S, et al. Among authors: mei s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Aug 10;35(4):471-474. doi: 10.3760/cma.j.issn.1003-9406.2018.04.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30098236 Chinese.

10

Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and homocystinuria.

Hu S, Mei S, Liu N, Kong X. Hu S, et al. Among authors: mei s. BMC Med Genet. 2018 Aug 29;19(1):154. doi: 10.1186/s12881-018-0666-x. BMC Med Genet. 2018. PMID: 30157807 Free PMC article.

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