HNRNPH2-Related Disorder Overview
Learn About HNRNPH2-Related Disorder
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Kristin Monaghan is a Medical Genetics provider in Detroit, Michigan. Dr. Monaghan and is rated as an Experienced provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Hypotonia, 1p36 Deletion Syndrome, Early Infantile Epileptic Encephalopathy, and KBG Syndrome.
Summary: Simons Searchlight is an observational, online, international research program for families with rare genetic variants that cause neurodevelopmental disorders and may be associated with autism. Simons Searchlight collects medical, behavioral, learning, and developmental information from people who have these rare genetic changes. The goal of this study is to improve the clinical care and treatment...