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A Novel CCND2 Mutation in a Previously Reported Case of Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and Hydrocephalus. [electronic resource] by
- Maini, I
- Farnetti, E
- Caraffi, S G
- Ivanovski, I
- De Bernardi, M L
- Gelmini, C
- Pollazzon, M
- Rosato, S
- Laurie, S
- Matalonga, L
- Baldo, C
- Garavelli, L
Producer: 20191008
In:
Neuropediatrics vol. 49
Availability: No items available.
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