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pro vyhledávání: '"Gabriela Monzoni"'
Autor:
Emanuel José Saad, Ayelén Tarditi Barra, Gabriela Monzoni, Carolina Villegas, Aldo Hugo Tabares
Publikováno v:
Revista de la Facultad de Ciencias Médicas de Córdoba, Vol 77, Iss 4 (2020)
Introduction: Sickle cell trait (SCT) is a rare and underdiagnosed disorder in the Argentinian population. In this condition, individuals carry the mutation of the HbS gene in one of the two beta-globin genes. In general, SCT does not present with th
Externí odkaz:
https://doaj.org/article/735c126861a645b9b49b421d3986da0f
Autor:
Gabriela Monzoni, Ayelén Tarditi Barra, Aldo H. Tabares, Carolina Villegas, Emanuel José Saad
Publikováno v:
Revista de la Facultad de Ciencias Médicas de Córdoba, Vol 77, Iss 4 (2020)
Introduction: Sickle cell trait (SCT) is a rare and underdiagnosed disorder in the Argentinian population. In this condition, individuals carry the mutation of the HbS gene in one of the two beta-globin genes. In general, SCT does not present with th