Publications

Found 4 results

Filters: Author is M.L. Ou [Clear All Filters]

2016

M. L. Ou, Liu, G., Xiao, D., Zhang, B. H., Guo, C. C., Ye, X. G., Liu, Y., Zhang, N., Wang, M., Han, Y. J., Ye, X. H., Jing, C. X., Yang, G., Ou, M. L., Liu, G., Xiao, D., Zhang, B. H., Guo, C. C., Ye, X. G., Liu, Y., Zhang, N., Wang, M., Han, Y. J., Ye, X. H., Jing, C. X., and Yang, G., “Association between miR-137 polymorphism and risk of schizophrenia: a meta-analysis”, vol. 15, p. -, 2016.

M. L. Ou, Liu, G., Xiao, D., Zhang, B. H., Guo, C. C., Ye, X. G., Liu, Y., Zhang, N., Wang, M., Han, Y. J., Ye, X. H., Jing, C. X., Yang, G., Ou, M. L., Liu, G., Xiao, D., Zhang, B. H., Guo, C. C., Ye, X. G., Liu, Y., Zhang, N., Wang, M., Han, Y. J., Ye, X. H., Jing, C. X., and Yang, G., “Association between miR-137 polymorphism and risk of schizophrenia: a meta-analysis”, vol. 15, p. -, 2016.

2015

C. C. Guo, Huang, W. H., Zhang, N., Dong, F., Jing, L. P., Liu, Y., Ye, X. G., Xiao, D., Ou, M. L., Zhang, B. H., Wang, M., Liang, W. K., Yang, G., and Jing, C. X., “Association between IL2/IL21 and SH2B3 polymorphisms and risk of celiac disease: a meta-analysis”, vol. 14, pp. 13221-13235, 2015.

S. X. Huang, Liang, J. L., Sui, W. G., Lin, H., Xue, W., Chen, J. J., Zhang, Y., Gong, W. W., Dai, Y., and Ou, M. L., “EDA mutation as a cause of hypohidrotic ectodermal dysplasia: a case report and review of the literature”, vol. 14, pp. 10344-10351, 2015.