Laura Bernardini
IRCCS Casa Sollievo della Sofferenza Foundation
6 papers found
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Delineation of MidXq28‐duplication syndrome distal to MECP2 and proximal to RAB39B genes
UploadEpilepsy phenotype in patients with Xp22.31 microduplication
Download from doi.orgSmall 4p16.3 deletions: Three additional patients and review of the literature
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