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CORC

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WHOLE EXOME SEQUENCE ANALYSIS IN PATIENTS WITH CERVICAL SEGMENTATION ABNORMALITIES IDENTIFIES KIAA1217 AS A CANDIDATE CAUSATIVE GENE 会议论文
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2019-04-01
作者:  Giampietro, P.;  Dhaheri, N. A.;  Blank, R.;  Raggio, C.;  Zhao, S.
收藏  |  浏览/下载：2/0  |  提交时间：2020/01/03
Whole-Exome Sequencing Analysis of One Patient with Synchronous AAH, MIA and IA 会议论文
作者:  Ma, K.;  Xu, Y.;  Cai, Y.;  Wang, X.
收藏  |  浏览/下载：6/0  |  提交时间：2019/12/05
Whole Exome Analysis of Incidental Tubal Precursors Without Concurrent Carcinomas 会议论文
MODERN PATHOLOGY, 2018-03-01
作者:  Lin, Shiou-Fu;  Jiao, Yuchen;  Wang, Tian-Li;  Shih, Ie-Ming
收藏  |  浏览/下载：3/0  |  提交时间：2020/01/03
WHOLE-EXOME SEQUENCING IDENTIFIES A CODING VARIANT IN SULT1A2 GENE ASSOCIATED WITH OBESITY IN CHINESE CHILDREN 会议论文
JOURNAL OF HYPERTENSION, 2018-10-01
作者:  Zhang, Meixian;  Li, Wenke;  Zhao, Xiaoyuan;  Gao, Liwang;  Wu, Lijun
收藏  |  浏览/下载：10/0  |  提交时间：2020/01/03
The Clinical Necessity of Extended Thymectomy for Thymic Squamous Cell Carcinomas Revealed by Exome Sequencing 会议论文
作者:  Jiang, J.;  Zhang, Y.;  Jin, C.;  Ding, J.
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/05
The Early Genetic Events in Cervical Cancers of Chinese Women and their Implications in Cancer Immunotherapy 会议论文
New horizons in cancer research, 中国上海
作者:  Xia Li;  Hailiang Huang;  Chen-Yi He;  Ming Qi;  Zhi-Ying Chen
收藏  |  浏览/下载：18/0  |  提交时间：2016/01/27
Exome sequencing identified emergence of HER2 kinase domain mutations in trastuzumab-resistant breast cancer 会议论文
作者:  Jiang, Yizhou;  Yu, Ke-Da;  Zuo, Wen-Jia;  Wang, Yu-Jie;  Shao, Zhi-Ming
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/13
EXOME SEQUENCE IDENTIFIES A NEW MUTATION OF PKHD1L1 IN A CHINESE FAMILY WITH CORTICAL TREMOR AND EPILEPSY 会议论文
作者:  Yu, P.;  Zhu, G.;  Ding, D.;  Xu, L.;  Ge, Y.
收藏  |  浏览/下载：1/0  |  提交时间：2019/12/19
Whole-exome sequencing identifies mutations in basonuclin 1 as a cause of premature ovarian failure 会议论文
作者:  Zhang, D.;  Zhang, Z.;  Lv, P. P.;  Liu, Y.;  Li, J. Y.
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/19
Whole-exome sequencing reveals a novel CHM gene mutation in a family with choroideremia initially diagnosed as retinitis pigmentosa 会议论文
第十四次全国医学遗传学学术会议
作者:  Hui Guo;  Ji-sheng Li;  Fei Gao;  Jiang-xia Li;  Qi-ji Liu
收藏  |  浏览/下载：10/0  |  提交时间：2019/12/31

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