Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 2 publications
SUPT16H-associated neurodevelopmental disorder and neurocristopathy: genetic and phenotypic spectrum.
Journal: Human molecular genetics
Published: November 07, 2025
De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities.
Journal: Journal of medical genetics
Published: April 01, 2019
Showing 1-2 of 2
Last Updated: 09/26/2026