Zobrazeno 1 - 2
of 2
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
Autor:
Billapati, Sushmitha1 (AUTHOR), Sowmya, G. C.1 (AUTHOR), Tapadia, R. S.1 (AUTHOR), Dutta, Usha R.2 (AUTHOR) ushadutta@hotmail.com
Publikováno v:
Egyptian Journal of Medical Human Genetics. 5/4/2022, Vol. 23 Issue 1, p1-4. 4p.