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頁籤選單縮合
題名 | Detection of Gene Deletions in Children with Chondrodysplasia Punctata, Ichthyosis, Kallmann Syndrome, and Ocular Albinism by FISH Studies=以螢光原位雜交法偵測斑點性軟骨形成不良、魚鱗癬、Kallmann氏症及眼白化症兒童之基因缺損 |
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作者姓名(中文) | 侯家瑋; | 書刊名 | 長庚醫學 |
卷期 | 28:9 民94.09 |
頁次 | 頁643-650 |
分類號 | 417.133 |
關鍵詞 | 相鄰基因症候群; 斑點性軟骨形成不良; 魚鱗癬; Kallmann氏症; 眼白化症; 螢光原位雜交法; Contiguous gene syndrome; Kallmann syndrome; Chondrodysplasia punctata; Ichthyosis; Ocular albinism; Fluorescence in situ hybridization; |
語文 | 英文(English) |