[1] |
Liu Tingting, Yang Fadeng, Lin Zhimiao, Wang Huijun, Hu Linghan, Zhong Weilong, Yang Yong.
Mutation analysis of the ABCA12 gene in two families with autosomal recessive congenital ichthyosis
[J]. Chinese Journal of Dermatology, 2018, 51(10): 737-740.
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[2] |
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Keratitis, ichthyosis, and deafness syndrome: a case report
[J]. Chinese Journal of Dermatology, 2017, 50(8): 599-601.
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[3] |
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Mutation analysis of the PNPLA1 gene in a family with autosomal recessive congenital ichthyosis
[J]. Chinese Journal of Dermatology, 2017, 50(6): 408-411.
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[4] |
Ying-Chun ZHANG Jian-Wei ZHU.
Female pattern hair loss in clinic
[J]. Chinese Journal of Dermatology, 2017, 50(10): 770-773.
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[5] |
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A case of keratitis-ichthyosis-deafness syndrome complicated by cutaneous squamous cell carcinoma: mutation analysis of the GJB2 gene and literature review
[J]. Chinese Journal of Dermatology, 2015, 48(12): 864-866.
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[6] |
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Phenotype, genotype and ultrastructural findings in a pedigree with autosomal recessive congenital ichthyosis
[J]. Chinese Journal of Dermatology, 2010, 43(8): 558-561.
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[7] |
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A case of ichthyosis linearis circumflexa
[J]. Chinese Journal of Dermatology, 2010, 43(8): 567-567.
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[8] |
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Diagnosis and treatment of porcupine-like ichthyosis: a case report
[J]. Chinese Journal of Dermatology, 2010, 43(11): 801-804.
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[9] |
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Genetic analysis of 1005 patients with vitiligo
[J]. Chinese Journal of Dermatology, 2010, 43(10): 684-686.
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[10] |
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A case of hidrotic ectodermal dysplasia accompanied by carpal maldevelopment
[J]. Chinese Journal of Dermatology, 2009, 42(1): 15-15.
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[11] |
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Transglutaminase 1 gene mutation in a family with lamellar ichthyosis
[J]. Chinese Journal of Dermatology, 2009, 42(1): 31-33.
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[12] |
ZHANG Xi-bao, WEI Sheng-cai, WANG Yan-fang, LI Chang-xing, XU Xiao, LI Ji, HE Yu-qing, LUO Quan.
The mutation of GJB2 gene in keratitis-ichthyosis-deafness syndrome
[J]. Chinese Journal of Dermatology, 2006, 39(3): 146-148.
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[13] |
WEI Sheng-cai, ZHENG Guang-yong, ZHANG Xi-bao, HUANG Zhen-ming, DENG Li, ZHANG Tang-de.
Transglutaminase 1 gene mutations in a family with lamellar ichthyosis
[J]. Chinese Journal of Dermatology, 2006, 39(3): 131-133.
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[14] |
XIA Yong-hua, LI Hong-wen, DING Yi.
The methylation of p16 promotor in psoriatic keratinocytes
[J]. Chinese Journal of Dermatology, 2006, 39(3): 128-130.
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[15] |
JIANG Yi-qun, CHEN Liu-qing, WU Li-ming, XU Xiu-lian, SUN Jian-fang.
Identification of DSRAD Gene Mutation in a Chinese Dyschromatosis Symmetrica Hereditaria Family
[J]. Chinese Journal of Dermatology, 2005, 38(4): 199-201.
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