ロード中...
5例Kallmann综合征患者的临床及遗传学分析
Kallmann syndrome (KS) is a rare pediatric disease with major manifestations of olfactory dysfunction and hypogonadotropic hypogonadism. Five children (4 boys and 1 girl) with KS reported in this article were aged between 6 months and 19 years at the time when they attended the hospital. All the chi...
保存先:
| 出版年: | Zhongguo Dang Dai Er Ke Za Zhi |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
中国当代儿科杂志编辑部
2018
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7389016/ https://ncbi.nlm.nih.gov/pubmed/30477624 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7499/j.issn.1008-8830.2018.11.009 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|