Nataliya Di Donato

Author Correction: Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia

Konrad Grützmann, Barbara Klink, Nadja Ehmke, 2018, Nature Communications.

Lissencephaly: Expanded imaging and clinical classification

Renzo Guerrini, William B Dobyns, A James Barkovich, 2017, American journal of medical genetics. Part A.

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.

Michael J Parker, Katrina Tatton-Brown, Christian Gilissen, 2015, American journal of human genetics.