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You searched for: Author/Creator Currò, Aurora- Currò, Aurora [remove] 4
- Human chromosome abnormalities -- Periodicals 2
- 572.8 1
- 616.0420 1
- 616.04205 1
- 616.13 1
- Human molecular genetics -- Periodicals 1
- IQSEC2 -- intellectual disability -- phenotype–genotype -- Rett syndrome 1
- Medical genetics -- Periodicals 1
- Mutation (Biology) -- Periodicals 1
- Slow-flow vascular malformations -- PIK3CA mutation -- non-invasive technique -- vascular system injuries -- cell-free DNA-next generation sequencing–liquid biopsy -- Klippel–Trenaunay syndrome 1