Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Shaozhen Mai"'
Autor:
Min Xu, Hui Xiong, Yanfang Han, Chijun Li, Shaozhen Mai, Zhongzhou Huang, Xuechen Ai, Zhixuan Guo, Fanqin Zeng, Qing Guo
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
Neurofibromatosis type I is a rare neurocutaneous syndrome resulting from loss-of-function mutations of NF1. The present study sought to determine a correlation between mutation regions on NF1 and the risk of developing optic pathway glioma (OPG) in
Externí odkaz:
https://doaj.org/article/5ab3e435ed7d4d34a18e4c6938b0a95d
Publikováno v:
European journal of dermatology : EJD. 28(1)
Autor:
Xu, Min, Xiong, Hui, Han, Yanfang, Li, Chijun, Mai, Shaozhen, Huang, Zhongzhou, Ai, Xuechen, Guo, Zhixuan, Zeng, Fanqin, Guo, Qing
Publikováno v:
Frontiers in Genetics; 7/24/2018, pN.PAG-N.PAG, 7p
Publikováno v:
European Journal of Dermatology; Jan/Feb2018, Vol. 28 Issue 1, p123-125, 3p, 1 Graph