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Modification of Hemoglobin H Disease by Sickle Trait
The rarity of hemoglobin (Hb) H disease in combination with sickle trait may be due in part to the absence of actual Hb H in individuals who, nonetheless, have inherited the deletion of three α-globin genes. We describe here a boy with persistent microcytic, hypochromic anemia despite adequate iron...
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| Yayımlandı: | J Clin Invest |
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| Asıl Yazarlar: | , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
American Society for Clinical Investigation
1979
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC372212/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/479366/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI109539 |
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