Zobrazeno 1 - 1
of 1
pro vyhledávání: '"G. C. Sowmya"'
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-4 (2022)
Abstract Background β-Thalassemia is an inherited haematological blood disorder in the HBB gene, and variations in this HBB gene lead to the absence/deficiency of the Beta chain synthesis of haemoglobin leading to severe anaemia. Klinefelter syndrom
Externí odkaz:
https://doaj.org/article/ebb037697da2415daa37c174284dc335
