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Punto de Vista | Junio 28, 2018

Carlos Cabrera entrevista a un grupo de miembros del Sickle Cell Thalassemia Patients Network (SCTPN) hablando sobre el síndrome de célula falciforme y como este grupo ayuda a pacientes en su diario vivir. En la segunda parte Carlos habla con la abogada Raquel Batista sobre temas de inmigración...

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