Alexandra Garza-Flores

Young Children With Gender Nonconforming Behaviors and Preferences.

E. Perrin, Marie Reilly, Vanessa Desousa, 2019, Journal of developmental and behavioral pediatrics : JDBP.

Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome

Ivan K. Chinn, R. Pfundt, B. D. de Vries, 2021, Genetics in Medicine.

Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.

P. Grant, N. Brunetti‐Pierri, D. Calame, 2022, American journal of human genetics.

Response to: Toriello et al., “Update on the Toriello–Carey Syndrome.” Further delineation of a young woman with deletion 1q42.12‐q42.2

A. Lin, M. Deardorff, J. Picker, 2017, American journal of medical genetics. Part A.