Angelo Selicorni
0000-0001-6187-3727
3 papers found
Refreshing results…
A missense mutation in DDRGK1 gene associated to Shohat‐type spondyloepimetaphyseal dysplasia: Two case reports and a review of literature
De novo heterozygous missense and loss‐of‐function variants in CDC42BPB are associated with a neurodevelopmental phenotype
Use of nutritional devices in Cornelia de Lange syndrome: Data from a large Italian cohort
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