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Human Genetics

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Publications

Neurodevelopmental and other phenotypes recurrently associated with heterozygous BAZ2B loss-of-function variants. Sewani, S; Azamian, MS; Mendelsohn, BA; Mau-Them, FT; Réda, M; Nambot, S; Isidor, B; van der Smagt, JJ; Shen, JJ; Shillington, A; Kinali, M; Zhao, X; Lalani, SR; Scott, DA. American Journal of Medical Genetics, Part A. 2024; 194:e63445.

P351: Genetic testing for patients with neurodevelopmental disorders in the inpatient psychiatry setting may reduce hospital stays and improve behavioral outcomes. Shillington, A; White, L; Doberstein, R; Hopkin, R; Harris, K; Zappia, K; Lamy, M. 2024; 2:101245.

Genetic syndromes are prevalent in patients with comorbid neurodevelopmental disorders and catatonia. Shillington, A; Zappia, KJ; White, L; Fosdick, C; Erickson, CA; Lamy, M; Dominick, KC. American Journal of Medical Genetics, Part A. 2023; 191:2716-2722.

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4.6
Overall Patient Rating