| 中国学者近期发表的论文 | |
|---|---|
| 1. | Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly. Author: Wang B, Li N, Geng J, Wang Z, Fu Q, Wang J, Xu Y. Journal: Congenit Anom (Kyoto). 2016 Jun 2. doi: 10.1111/cga.12173. [Epub ahead of print] |
| 2. | Clinical study of 459 polydactyly cases in China, 2010 to 2014. Author: Xiang Y, Bian J, Wang Z, Xu Y, Fu Q. Journal: Congenit Anom (Kyoto). 2016 Mar 8. doi: 10.1111/cga.12163. [Epub ahead of print] |
| 3. | Expression of peptide fragments from proADM and involvement of mitogen-activated protein kinase signaling pathways in pulmonary remodeling induced by high pulmonary blood flow. Author: Li W, Guo A, Wang L, Kong Q, Wang R, Han L, Zhao C. Journal: Congenit Anom (Kyoto). 2016 Jan;56(1):28-34. doi: 10.1111/cga.12114. |
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