ロード中...
Acute Dystonia in a Patient with 22q11.2 Deletion Syndrome
The 22q11.2 deletion syndrome (di George syndrome) is one of the most prevalent genetic disorders. The clinical features of the syndrome are distinct facial appearance, velopharyngeal insufficiency, conotruncal heart disease, parathyroid and immune dysfunction; however, little is known about possibl...
保存先:
| 出版年: | Ment Illn |
|---|---|
| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
PAGEPress Publications, Pavia, Italy
2015
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4620283/ https://ncbi.nlm.nih.gov/pubmed/26605035 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4081/mi.2015.5902 |
| 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!
|