Williams Syndrome

Defining the Brain Phenotype of Children With Williams Syndrome

Williams Syndrome (WS) and Supravalvar Aortic Stenosis (SVAS) DNA and Tissue Bank

Impact of Elastin Mediated Vascular Stiffness on End Organs

A Case-Control Observational Study of Peripheral Blood-Derived iPSC Models to Investigate Oligodendrocyte Lineage Development in Children With Williams Syndrome and Healthy Controls

Intensive Multimodal Neurorehabilitation Targeting Neuroplasticity in Pediatric Neurodevelopmental and Chromosomal Disorders

Clemastine Fumarate in the Treatment of Neurodevelopmental Delays in Williams Syndrome

The Psychiatric and Cognitive Phenotypes in Velocardiofacial Syndrome

WS-SAVE Study (Williams Syndrome Skin and Vessel Elasticity Study)

Clemastine Treatment in Individuals With Williams Syndrome

Physical Activity and Community EmPOWERment Project

Phonological Constraints on Language Development in Individuals With Williams Syndrome

Parent and Infant Inter(X)Action Intervention (PIXI)

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

Characterization and Natural History of Williams Syndrome and Other Chromosome 7q11.23 Variants

Buspirone Treatment of Anxiety in Williams Syndrome

Motor Deficits and Signal Conduction in Individuals With Williams Syndrome

Williams Syndrome Strength, Hormones, Activity & Adiposity, DNA Programming, Eating Study

Cooperative Parent Mediated Therapy in Children With Fragile X Syndrome and Williams Syndrome

Cognitive and Behavioral Therapy of Anxiety in Williams Syndrome

Response Inhibition Training for Children With Williams Syndrome