[1] |
Li Bo, Wen Guangdong, Yu Cong, Zhang Jianzhong, Zhou Cheng.
Gene mutation analysis of a family with familial generalized lentiginosis
[J]. Chinese Journal of Dermatology, 2022, 55(2): 146-149.
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[2] |
Liu Yihe, Chen Zhiming, Feng Suying, Yang Yong.
A case of ADULT syndrome without finger/toe deformities caused by a TP63 mutation
[J]. Chinese Journal of Dermatology, 2022, 0(2): 20210554-e20210554.
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[3] |
Yang Rui, Kong Qingtao, Xu Jie, Zhang Chen, Sang Hong.
Screening of susceptibility genes and an immunological study in a patient with recurrent cervical lymphadenitis caused by Candida albicans
[J]. Chinese Journal of Dermatology, 2022, 55(1): 50-54.
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[4] |
Yang Lu, Duan Zhimin, Li Min.
Mechanisms underlying the resistance of Candida albicans to echinocandin antifungals
[J]. Chinese Journal of Dermatology, 2022, 0(1): 20210273-e20210273.
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[5] |
Chen Yingdan, Huang Hui, Luo Shuaihantian, Li Yaping, Shi Xiaoliu, Zhang Guiying.
A case of atypical late-onset Netherton syndrome without bamboo hair
[J]. Chinese Journal of Dermatology, 2021, 54(8): 716-718.
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[6] |
He Tianrong, Liu Yunqiang, Yang Yuan.
A study on pathogenicity of TGM1 gene mutations in a collodion baby
[J]. Chinese Journal of Dermatology, 2021, 54(8): 712-715.
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[7] |
Liu Yihe, Chen Zhiming, Yang Yong.
Chanarin-Dorfman syndrome: the first case reported in China
[J]. Chinese Journal of Dermatology, 2021, 54(8): 673-676.
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[8] |
Wu Yali, Mei Juan, Zhao Lingxia, Yin Wei.
A de novo mutation in the PORCN gene in a newborn with Goltz syndrome
[J]. Chinese Journal of Dermatology, 2021, 54(6): 514-517.
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[9] |
Yang Zhou, Xu Zhe, Ma Lin.
Analysis of 12R-lipoxygenase gene mutations in three families with self-improving collodion ichthyosis
[J]. Chinese Journal of Dermatology, 2021, 54(5): 397-401.
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[10] |
Guo Yiyan, Zhou Taicheng, Li Gaiying, Luo Xuan, Wang Ruiqi, Ma Yiqun, Jiang Yan, Tang Yang.
Correlation between mitochondrial DNA control region variations and keloid formation
[J]. Chinese Journal of Dermatology, 2021, 54(5): 421-427.
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[11] |
Wang Xiaopo, Chen Zhiming, Yang Yong, Sun Jianfang .
A family of severe epidermolysis bullosa simplex caused by a de novo mutation in the KRT5 gene
[J]. Chinese Journal of Dermatology, 2021, 54(3): 229-231.
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[12] |
Wang Jianbo, Li Zhenlin, Dou Jinfa, Qin Zheng, Wu Shuping, Zhang Shoumin, Xu Yuping, Li Zhenlu.
Gene mutation analysis in a Chinese pedigree with autosomal recessive woolly hair
[J]. Chinese Journal of Dermatology, 2021, 54(2): 145-147.
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[13] |
Yang Zhou, Xu Zhe, Wang Zhaoyang, Chen Yunliu, Ma Lin.
TP63 gene mutation analysis in a case of ankyloblepharon-ectodermal dysplasia-clefting syndrome
[J]. Chinese Journal of Dermatology, 2021, 0(2): 20201051-e20201051.
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[14] |
Qin Bei, Li Qinfeng, Lian Jia.
An infant with lamellar ichthyosis induced by CYP4F22 gene mutations
[J]. Chinese Journal of Dermatology, 2021, 54(12): 1096-1098.
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[15] |
Liu Liqin, Wang Jinyan, Jiao Ting, Zhang Li, Han Changyuan, Ye Yingyi.
Mutation analysis of the PTPN11 gene in a pedigree with LEOPARD syndrome
[J]. Chinese Journal of Dermatology, 2021, 54(11): 998-1000.
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