Difference between revisions of "DICER1 syndrome"
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Revision as of 20:25, 21 August 2018
DICER1 syndrome is characterized by mutations in the DICER1 gene.
Tumour associated with the syndrome include:
References
- ↑ 1.0 1.1 van Engelen, K.; Villani, A.; Wasserman, JD.; Aronoff, L.; Greer, MC.; Tijerin Bueno, M.; Gallinger, B.; Kim, RH. et al. (Jan 2018). "DICER1 syndrome: Approach to testing and management at a large pediatric tertiary care center.". Pediatr Blood Cancer 65 (1). doi:10.1002/pbc.26720. PMID 28960912.