遗传与出生缺陷疾病研究组

Laboratory of Inherited Disorders and Birth Defects

发表论文
1.

Chen J #, Wang Q#,, Cabrera PE, Zhong Z, Sun W, Jiao X, Chen Y, Govindarajan G, Naeem MA, Khan SN, Ali MH, Assir MZ, Rahman FU, Qazi ZA, Riazuddin S, Akram J, Riazuddin SA, Hejtmancik JF*. Molecular Genetic Analysis of Pakistani Families With Autosomal Recessive Congenital Cataracts by Homozygosity Screening. Invest Ophthalmol Vis Sci. 2017 Apr 1;58(4):2207-2217.

2.

Zhong Z, Wu Z, Han L, Chen J*. Novel mutations in CRYGC are associated with congenital cataracts in Chinese families. Sci Rep. 2017 Mar 15; 7(1):189.

3.

Wang J, Gao F, Li J, Zhang J, Li S, Xu GT, Xu L, Chen J, Lu L*. The usability of WeChat as a mobile and interactive medium in student-centered medical teaching. Biochem Mol Biol Educ. 2017 Sep;45(5):421-425.

4.

Li L#, Chen Y#, Jiao X, Jin C, Jiang D, Tanwar M, Ma Z, Huang L, Ma X, Sun W, Chen J, Ma Y, M'hamdi O, Govindarajan G, Cabrera PE, Li J, Gupta N, Naeem MA, Khan SN, Riazuddin S, Akram J, Ayyagari R, Sieving PA, Riazuddin SA, Hejtmancik JF*. Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families. Invest Ophthalmol Vis Sci. 2017 Apr 1;58(4):2218-2238.

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chenjianjun@tongji.edu.cn

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