Abstract
Objective: To evaluate vitrification and controlled-rate freezing of murine blastocysts. For optimal survival and implantation potential, human blastocysts at varying developmental stages from the same cohort may need to be frozen at different times. Multiple freezing procedures/patient can be costly, disruptive to workflow, and impractical with standard controlled-rate freezing, since each freeze requires considerable time to perform. Rapid freezing methods including vitrification could overcome these problems.
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