CORC

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CORC

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Profiling Receptor Tyrosine Kinase Fusions in Chinese Breast Cancers 期刊论文
FRONTIERS IN ONCOLOGY, 2021, 卷号: 11
作者:  Tao, Zhonghua;  Liu, Jianxia;  Li, Ting;  Xu, Hong;  Chen, Kai
收藏  |  浏览/下载：33/0  |  提交时间：2022/01/10
C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients 期刊论文
MOLECULAR MEDICINE REPORTS, 2017, 卷号: 16, 页码: 5333-5337
作者:  Lin, Ying[1];  Gao, Hongbin[2,3];  Ai, Siming[1];  Eswarakumar, Jacob V. P.[4];  Chen, Chuan[1,5]
收藏  |  浏览/下载：2/0  |  提交时间：2019/04/24
S267P Mutation in FGFR2: First Report in a Patient With Crouzon Syndrome 期刊论文
JOURNAL OF CRANIOFACIAL SURGERY, 2015, 卷号: 26, 期号: 2
作者:  Ke, Ronghu;  Yang, Xianxian;  Ge, Min;  Cai, Tianyi;  Lei, Jiaqi
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/13
The C342R Mutation in FGFR2 Causes Crouzon Syndrome With Elbow Deformity 期刊论文
JOURNAL OF CRANIOFACIAL SURGERY, 2015, 卷号: 26, 期号: 2
作者:  Ke, Ronghu;  Yang, Xianxian;  Cai Tianyi;  Ge, Min;  Lei, Jiaqi
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/19
De novo GLI3 mutation in esophageal atresia: Reproducing the phenotypic spectrum of Gli3 defects in murine models 期刊论文
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2014, 卷号: 1842, 期号: 9, 页码: 1755-1761
Yang, L; Shen, C; Mei, M; Zhan, GD; Zhao, YK; Wang, HJ; Huang, GY; Qiu, ZL; Lu, WN; Zhou, WH
收藏  |  浏览/下载：39/0  |  提交时间：2014/12/15
[FGFR2 gene mutation in a Chinese patient with Apert syndrome]. 期刊论文
Chinese Journal Of Medical Genetics, 2010, 卷号: Vol.27 No.6, 页码: 682-684
作者:  Dai L;  Li NN;  Yuan YM;  Liu Y;  Zhu J
收藏  |  浏览/下载：1/0  |  提交时间：2019/03/26
A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis 期刊论文
Bone, 2008, 卷号: Vol.42 No.4, 页码: 631-643
作者:  Liangjun Yin;  Xiaolan Du;  Cuiling Li;  Xiaoling Xu;  Zhi Chen
收藏  |  浏览/下载：2/0  |  提交时间：2019/02/25

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