Suppr超能文献

Genetic sequencing of a patient with Kallmann syndrome plus 5α-reductase type 2 deficiency.

作者信息

Ji Wen, Zhang Lu-Yao, Li Fu-Cheng, Wang Yu, He Wei, Yin Qi-Qi, Liao Zhi-Hong

机构信息

Department of Endocrinology, 1st Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510080, China.

Department of Medical Genetics, Genome Research Center, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, China.

出版信息

Asian J Androl. 2017 May-Jun;19(3):386-387. doi: 10.4103/1008-682X.170865.

Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f2e/5427800/d8203b322fc8/AJA-19-386-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验