6 results on '"Drera, B."'
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2. De novo occurrence of the 730insG recurrent mutation in an Italian family with the ichthyotic variant of Vohwinkel syndrome, loricrin keratoderma
3. Recurrence of the p.R156X TNNI2 mutation in distal arthrogryposis type 2B
4. Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization
5. Identification of a novel TGFBR1 mutation in a Loeys–Dietz syndrome type II patient with vascular Ehlers–Danlos syndrome phenotype
6. De novo occurrence of the 730insG recurrent mutation in an Italian family with the ichthyotic variant of Vohwinkel syndrome, loricrin keratoderma
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