Search Results - "Deciphering Developmental Disorders Study"

Extending the phenotype associated with the CSNK2A1‐related Okur–Chung syndrome—A clinical study of 11 individuals.

Authors: Owen, Ceris I. Bowden, Ramsay Parker, Michael J. et al.

Source: American Journal of Medical Genetics. Part A; May2018, Vol. 176 Issue 5, p1108-1114, 7p