Andrea Accogli
0000-0001-8724-6721
3 papers found
Refreshing results…
Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals
L1CAM variants cause two distinct imaging phenotypes on fetal MRI
De novo heterozygous missense and loss‐of‐function variants in CDC42BPB are associated with a neurodevelopmental phenotype
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