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Contribution of intragenic deletions to mutation spectrum in Chinese patients with Wilson's disease and possible mechanism underlying ATP7B gross deletions 期刊论文
PARKINSONISM & RELATED DISORDERS, 2019, 卷号: 62
作者:  Chen, Yu-Chao;  Yu, Hao;  Wang, Rou-Min;  Xie, Juan-Juan;  Ni, Wang
收藏  |  浏览/下载:24/0  |  提交时间:2019/12/05
Clinical and biochemical consequences of an intragenic growth hormone receptor (GHR) deletion in a large Chinese pedigree 期刊论文
CLINICAL ENDOCRINOLOGY, 2015, 卷号: 82, 期号: 3
作者:  Klammt, Juergen;  Shen, Shuixian;  Kiess, Wieland;  Kratzsch, Juergen;  Stobbe, Heike
收藏  |  浏览/下载:7/0  |  提交时间:2019/12/19
Alu-specific microhomology-mediated deletion of the final exon of SPAST in three unrelated subjects with hereditary spastic paraplegia 期刊论文
GENETICS IN MEDICINE, 2011, 卷号: 13, 期号: 6
作者:  Boone, Philip M.;  Liu, Pengfei;  Zhang, Feng;  Carvalho, Claudia M. B.;  Towne, Charles F.
收藏  |  浏览/下载:7/0  |  提交时间:2019/12/19
Intragenic deletion of tgif causes defects in brain development 期刊论文
Human molecular genetics, 2006, 卷号: 15, 期号: 24, 页码: 3508-3519
作者:  Kuang, Chenzhong;  Xiao, Yan;  Yang, Ling;  Chen, Qian;  Wang, Zhenzhen
收藏  |  浏览/下载:24/0  |  提交时间:2019/05/10


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