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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...
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| Gepubliceerd in: | Zhongguo Dang Dai Er Ke Za Zhi |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
中国当代儿科杂志编辑部
2018
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| Onderwerpen: | |
| Online toegang: | 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 |
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