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CORC

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In vitro and in vivo studies on magnesium alloys to evaluate the feasibility of their use in obstetrics and gynecology 期刊论文
2019
作者:  Bao Guo;  Fan Qianqian;  Ge Dongfeng;  Sun Mingming;  Guo Hui
收藏  |  浏览/下载：5/0  |  提交时间：2020/01/03
The first case of primary hypertrophic osteoarthropathy with soft tissue giant tumors caused by HPGD loss-of-function mutation 期刊论文
2019, 卷号: 8, 期号: 6, 页码: 736-744
作者:  Pang, Qianqian;  Xu, Yuping;  Qi, Xuan;  Jiang, Yan;  Wang, Ou
收藏  |  浏览/下载：9/0  |  提交时间：2020/01/03
Clinical and genetic analysis in a large Chinese cohort of patients with X-linked hypophosphatemia 期刊论文
2019, 卷号: 121, 页码: 212-220
作者:  Zhang, Cong;  Zhao, Zhen;  Sun, Yue;  Xu, Lijun;  JiaJue, Ruizhi
收藏  |  浏览/下载：13/0  |  提交时间：2020/01/03
Four novel mutations in the ALPL gene in Chinese patients with odonto, childhood, and adult hypophosphatasia 期刊论文
2018, 卷号: 38, 期号: 4
作者:  Xu, Lijun;  Pang, Qianqian;  Jiang, Yan;  Wang, Ou;  Li, Mei
收藏  |  浏览/下载：3/0  |  提交时间：2020/01/03
ALPL gene  HPP  TNSALP  
Identification of mutations in the prostaglandin transporter gene SLCO2A1 and phenotypic comparison between two subtypes of primary hypertrophic osteoarthropathy (PHO): A single-center study 期刊论文
2018, 卷号: 106, 页码: 96-102
作者:  Hou, Yanfang;  Lin, Yuanyuan;  Qi, Xuan;  Yuan, Lu;  Liao, Ruoxi
收藏  |  浏览/下载：3/0  |  提交时间：2020/01/03
Familial Early-Onset Paget's Disease of Bone Associated with a Novel hnRNPA2B1 Mutation 期刊论文
2017, 卷号: 101, 期号: 2, 页码: 159-169
作者:  Qi Xuan;  Pang Qianqian;  Wang Jiawei;  Zhao Zhen;  Wang Ou
收藏  |  浏览/下载：3/0  |  提交时间：2020/01/04
Identification of suitable reference gene and biomarkers of serum miRNAs for osteoporosis 期刊论文
2016, 卷号: 6, 页码: 36347
作者:  Chen, Jian;  Li, Kai;  Pang, Qianqian;  Yang, Chao;  Zhang, Hongyu
收藏  |  浏览/下载：1/0  |  提交时间：2020/01/04
Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets 期刊论文
2016, 卷号: 4, 期号: 1, 页码: 16018
作者:  Pang, Qianqian;  Qi, Xuan;  Jiang, Yan;  Wang, Ou;  Li, Mei
收藏  |  浏览/下载：1/0  |  提交时间：2020/01/04
Novel COL2A1 mutations causing spondyloepiphyseal dysplasia congenita in three unrelated Chinese families 期刊论文
2016, 卷号: 25, 期号: 9, 页码: 2967-2974
作者:  Liu, Limin;  Pang, QianQian;  Jiang, Yan;  Li, Mei;  Wang, Ou
收藏  |  浏览/下载：3/0  |  提交时间：2020/01/04
First Report of a Novel Missense CLDN19 Mutations Causing Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis in a Chinese Family 期刊论文
2015, 卷号: 96, 期号: 4, 页码: 265-273
作者:  Yuan, Tao;  Pang, Qianqian;  Xing, Xiaoping;  Wang, Xi;  Li, Yuhui
收藏  |  浏览/下载：2/0  |  提交时间：2020/01/13

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