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Hemoglobin H disease due to a de novo mutation at the α2-globin gene and an inherited common α-thalassemia deletion found in a Chinese boy
✍ Scribed by Chunjiang Zhu; Wenfang Yu; Jiansheng Xie; Ling Chen; Hui Ding; Xuan Shang; Xiangmin Xu
- Book ID
- 116304796
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 387 KB
- Volume
- 45
- Category
- Article
- ISSN
- 1079-9796
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