| 缩写名/全名 |
CONGENIT ANOM
CONGENITAL ANOMALIES |
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| ISSN号 | 0914-3505 | ||||||||||
| 研究方向 | PEDIATRICS- | ||||||||||
| 影响因子 | 2015:0.985, 2016:1.537, 2017:1.149, 2018:1.23, 2019:1.761, | ||||||||||
| 出版国家 | JAPAN | ||||||||||
| 出版周期 | |||||||||||
| 年文章数 | 31 | ||||||||||
| 出版年份 | 0 | ||||||||||
| 是否OA | No | ||||||||||
| 审稿周期(仅供参考) | |||||||||||
| 录用比例 | |||||||||||
| 投稿链接 | https://mc.manuscriptcentral.com/cga | ||||||||||
| 投稿官网 | http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1741-4520 | ||||||||||
| h-index | 25 | ||||||||||
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| PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=0914-3505%5BISSN%5D | ||||||||||
| 中科院SCI期刊分区 （ 2018年新版本） |
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| 中科院SCI期刊分区 （ 2020年新版本） |
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| 中国学者近期发表的论文 | |
| 1. | 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. PubMed |
| 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] PubMed |
| 3. | 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] PubMed |
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