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Author/Creator Pan, Chaolan

4. Focal facial dermal dysplasias type III: Two families with Setleis syndrome in China. Issue 10 (17th June 2022)

Authors:
Cao, Qiaoyu; Zhang, Shuai; Wang, Jianbo; Wang, Yumeng; Pan, Chaolan; Wang, Xinyi; Zhao, Anqi; Chen, Xiao; Qin, Pingping; Zhang, Shoumin; Yao, Zhirong; Lv, Dong; Yang, Yali; Li, Ming
Journal:
Journal of dermatology
Issue:
Volume 49:Issue 10(2022)
Page Start:
1057
Record Type:
Journal Article
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5. Genotype and phenotype correlations in 441 patients with epidermolysis bullosa from China. (5th November 2022)

Authors:
Chen, Fuying; Wei, Ruoqu; Deng, Dan; Zhang, Xue; Cao, Yu; Pan, Chaolan; Wang, Yumeng; Cao, Qiaoyu; Wang, Jianbo; Zeng, Ming; Huang, Linting; Gu, Yan; Yao, Zhirong; Li, Ming
Journal:
Journal of the European Academy of Dermatology and Venereology
Issue:
Volume 37:Number 2(2023)
Page Start:
411
Record Type:
Journal Article
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6. Netherton syndrome caused by compound heterozygous mutation, c.80A>G mutation in SPINK5 and large‐sized genomic deletion mutation, and successful treatment of intravenous immunoglobulin. Issue 3 (16th January 2021)

Authors:
Zhang, Zhen; Pan, Chaolan; Wei, Ruoqu; Li, Huaguo; Yang, Yijun; Chen, Jiawen; Li, Ming; Yao, Zhirong
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 9:Issue 3(2021)
Page Start:
n/a
Record Type:
Journal Article
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7. S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis‐like syndrome. Issue 5 (1st April 2022)

Authors:
Chen, Fuying; Ni, Cheng; Wang, Xiaoxiao; Cheng, Ruhong; Pan, Chaolan; Wang, Yumeng; Liang, Jianying; Zhang, Jia; Cheng, Jinke; Chin, Y Eugene; Zhou, Yi; Wang, Zhen; Guo, Yiran; Chen, She; Htun, Stephanie; Mathes, Erin F; de Alba Campomanes, Alejandra G; Slavotinek, Anne M; Zhang, Si; Li, Ming
Journal:
EMBO molecular medicine
Issue:
Volume 14:Issue 5(2022)
Page Start:
n/a
Record Type:
Journal Article
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