טוען...
新疆维吾尔族儿童21-羟化酶缺乏症基因型与表型的研究
OBJECTIVE: To investigate gene mutations and the relationship between genotypes and clinical phenotypes in Uygur children with 21-hydroxylase deficiency(21-OHD) in Xinjiang, China. METHODS: A total of 20 Uygur children with 21-OHD who visited the hospital between October 2013 and October 2014 were e...
שמור ב:
| הוצא לאור ב: | Zhongguo Dang Dai Er Ke Za Zhi |
|---|---|
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
中国当代儿科杂志编辑部
2016
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7403052/ https://ncbi.nlm.nih.gov/pubmed/26903061 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7499/j.issn.1008-8830.2016.02.009 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|