Margaret J Wilkes

Loeys–Dietz syndrome caused by 1q41 deletion including TGFB2 is associated with a neurodevelopmental phenotype

M. Tucker, Erin M. Demo, G. MacCarrick, 2022, American journal of medical genetics. Part A.

Inherited Retinal Dystrophy in Southeastern United States: Characterization of South Carolina Patients and Comparative Literature Review

E. Say, G. Magrath, Kareem Sioufi, 2022, Genes.