基于综合嵌合突变分析技术的节段型1型神经纤维瘤病的诊断策略及局部神经纤维瘤发生规律的探究
序号 | 标题 | 类型 | 作者 |
---|---|---|---|
1 | Halo-like phenomenon in neurofibromatosis type 1: A potential new diagnostic criterion. | 期刊论文 | Jia Zhang;Qianyue Xu;Jinwen Shen;Ming Li;Zhirong Yao |
2 | Cafe au lait macules overlying segmental macular hyperpigmentation in a paediatric patient: an early sign for mosaic neurofibromatosis type 1 | 期刊论文 | Zhang J;Qin W;Hua S;Li M;Tang Y;Yao Z |
3 | 华夏医学科技奖一等奖 | 奖励 | 姚志荣;徐金华;顾恒;李明;郭一峰;李化国;张卉;程茹虹;余红;张佳;鲁智勇;余霞;沈瑾文;倪成;顾艳 |
4 | Novel mutations in Chinese hypotrichosis simplex patients associated with LSS gene | 期刊论文 | Hua Shengyuan;Ding Yu;Zhang Jia;Qian Qiufang;Li Ming |
5 | 一例有节段型咖啡斑表现患儿的镶嵌变异研究 | 期刊论文 | 丁钰;华圣元;方碧清;张佳 |
6 | Two cases of pityriasis rosea after the injection of coronavirus disease 2019 vaccine | 期刊论文 | Huang L;Yao Z;Zhang J |
7 | Novel splice site mutation at the C‐terminal of SPINK5 cause a unique Netherton syndrome phenotype mimicking pustular psoriasis | 期刊论文 | Shengyuan Hua;Jing Liu;Biqing Fang;Qiufang Qian;Jia Zhang |