Prasad, Asuri N

Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype

Prasad, C., Prasad, A. N., Chodirker, B. N., Lee, C., Dawson, A. K., Jocelyn, L. J., & Chudley, A. E. (2000) · Clinical Genetics

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

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Psychosocial Correlates of Neurodevelopmental Disabilities in 2- to 3-Year-Olds

Fitneva, S. A., Corbett, B. A., & Prasad, A. N. (2023) · Epilepsy & Behavior

Autism Spectrum Disorder ResearchFamily and Disability Support Research

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