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AAMAC Webinar - A Review of the Stem Cell Registry
Rare Disease Day takes place on the last day of February each year. The main objective is to raise awareness amongst the general public and decision-makers about rare diseases and their impact on patients' lives. This year it is on February 29, the rarest day of the year! Join AAMAC on Saturday February 29, 2020 for an informative webinar Time: 1pm – 2pm (EASTERN TIME) Speaker: Dr. Heidi Elmoazzen – director, stem cells at Canadian Blood Services Topic: How the Stem Cell Registry is managed Visit https://aamac.ca/meeting-events/ to register
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Aplastic Anemia & Myelodysplasia Association of Canada | Association canadienne de l'anemie aplasique et de la myelodysplasie www.aamac.ca 1-888-840-0039 Last edited by Neil Cuadra : Tue Feb 11, 2020 at 02:09 PM. Reason: fixed syntax error in image URL |
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How the Stem Cell Registry is Managed?
Are you interested in hearing more about how the stem cell registry is managed?
In celebration of Rare Disease Day join AAMAC’s Webinar today – 1pm – 2pm (Eastern Time) led by a director, stem cells at Canadian Blood Services It is not too late to register at https://aamac.ca/events/webinar-february-29-2020/ #rarediseaseday #rallyforrare
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Aplastic Anemia & Myelodysplasia Association of Canada | Association canadienne de l'anemie aplasique et de la myelodysplasie www.aamac.ca 1-888-840-0039 |
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