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浏览/检索结果: 共5条，第1-5条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Marie Unna hereditary hypotrichosis accompanied by multiple familial trichoepithelioma in a Chinese family 期刊论文 2019, 卷号: 46, 期号: 5, 页码: 413-417 作者:  Huang, Ye;  Cai, Chuan;  Ren, Li;  Cui, Caijuan;  Zhang, Xue 收藏  |  浏览/下载：10/0  |  提交时间：2020/01/03 HR  fatty acid-binding protein 12  genetic variant  Marie Unna hereditary hypotrichosis  multiple familial trichoepithelioma   A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis 期刊论文 2018, 卷号: 138, 期号: 1, 页码: 230-233 作者:  Yu, Xia;  Chen, Fuyin;  Ni, Cheng;  Zhang, Guolong;  Zheng, Luyao 收藏  |  浏览/下载：5/0  |  提交时间：2020/01/03 ADWH/hypotrichosis  KRT25  autosomal dominant  whole exome sequencing   Exome sequencing reveals novel BCS1L mutations in siblings with hearing loss and hypotrichosis 期刊论文 Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function, 2015, 卷号: 566, 期号: 1, 页码: 84-88 作者:  Zhang, Jie;  Duo, Lina;  Lin, Zhimiao;  Wang, Huijun;  Yin, Jinghua 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/17 Exome sequencing  Hearing loss  Hypotrichosis  BCS1L gene  Bjornstad syndrome   A novel missense mutation in lipase H (LIPH) gene in a Chinese people with woolly hair/hypotrichosis 期刊论文 JOURNAL OF DERMATOLOGY, 2012, 卷号: 39, 期号: [db:dc_citation_issue], 页码: 200-200 作者:  Ma Jun-hong;  Wang Xin;  Xiao Sheng-xiang 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/10 A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12 similar to 12.3 in a Chinese family 期刊论文 JOURNAL OF CUTANEOUS PATHOLOGY, 2010, 卷号: 37, 期号: 7, 页码: 758-763 作者:  Xu, Chao;  Zhang, Li;  Chen, Nan;  Su, Bin;  Pan, Cun-Ming 收藏  |  浏览/下载：5/0  |  提交时间：2019/12/26