Alessandro Ferraris
1PUBLICATIONS
3CO-AUTHORS

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Publications (1)
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|Dec 23, 2022
Congenital Defects in a Patient Carrying a Novel Homozygous <i>AEBP1</i> Variant: Further Expansion of the Phenotypic Spectrum of Ehlers-Danlos Syndrome Classical-like Type 2?Niccolò Di Giosaffatte, Alessandro Ferraris, Federica Gaudioso
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