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α-Thalassemia in the American Negro

In Italian and Chinese patients with the α-thalassemia syndromes the production of α-chain of normal hemoglobin is decreased relative to that of β-chain in reticulocytes. In this study the relative rates of α- and β-chain synthesis were determined in members of three Negro families with α-thalassemi...

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Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Schwartz, Elias, Atwater, Jean
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1972
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC302140/
https://ncbi.nlm.nih.gov/pubmed/5061833
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