ロード中...
Genome-wide analysis of Ollier disease: Is it all in the genes?
BACKGROUND: Ollier disease is a rare, non-hereditary disorder which is characterized by the presence of multiple enchondromas (ECs), benign cartilaginous neoplasms arising within the medulla of the bone, with an asymmetric distribution. The risk of malignant transformation towards central chondrosar...
保存先:
| 主要な著者: | , , , , , , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2011
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3027091/ https://ncbi.nlm.nih.gov/pubmed/21235737 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-6-2 |
| 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!
|