Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID. February 24, 2015 DYRK1A Read Full Read more
A de novo 1.4-Mb deletion at 21q22.11 in a boy with developmental delay January 23, 2014 DYRK1A Read Abstract Read more
The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy October 25, 2012 DYRK1A Read Abstract Read more
Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly March 1, 2011 DYRK1A Read Abstract Read more
Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A September 14, 2010 DYRK1A Read Full Read more
Truncation of the Down Syndrome Candidate Gene DYRK1A in Two Unrelated Patients with Microcephaly May 1, 2008 DYRK1A Read Full Read more
