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一种新的3.8 kb缺失α地贫基因的鉴定
OBJECTIVE: To report the identification of a novel 3.8-kb deletion that caused α thalassemia and establish the method for detecting the deletion fragment. METHODS: Peripheral blood samples were collected from the proband and his mother for analysis of the hematological parameters and routine test fo...
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| Publicat a: | Nan Fang Yi Ke Da Xue Xue Bao |
|---|---|
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
南方医科大学学报编辑部
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6765508/ https://ncbi.nlm.nih.gov/pubmed/28736383 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3969/j.issn.1673-4254.2017.07.26 |
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