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PB2047: MOLECULAR DIAGNOSIS OF CONGENITAL ERYTHROCYTOSIS IN A SINGLE HOSPITAL CENTER.

Detalles Bibliográficos
Autores principales:	Castilla Garcia, L., Aspa Cilleruelo, J. M., Lopez de Hontanar Torres, G., Rodriguez Barquero, P. A., Sánchez Perez, R., Ayala Diaz, R., Ropero Gradilla, P., Martínez Nieto, J., González Fernández, A., Argüello Marina, M., Lopez Rubio, M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2022
Materias:	Publication Only
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9429399/ http://dx.doi.org/10.1097/01.HS9.0000851020.96678.86

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