ASXL3 Mutations &
Bainbridge-Ropers Syndrome
Current ASXL3 Research
Simons VIP Connect ASXL3 Study
From the Simons VIP Connect Website: The Simons Variation in Individuals Project - Simons VIP - is an online community that supports families with rare genetic changes (also called “genomic variants”) associated with features of autism and developmental delay. We provide access to resources, information, and family support. Simons VIP also provides an opportunity for families to participate in research.
SPARK for Autism
From the SPARK for Autism Website: The mission of SPARK — an online research partnership involving 50,000 individuals with autism and their families — is simple. We want to speed up research and advance understanding of autism.
Help us spark better futures for all individuals and families affected by autism. Click here for the SPARK website.
Clinical Registry for Bohring-Opitz Syndrome & Other ASXL-Related Phenotypes
Registry created by the Cincinnati Children's Hospital Medical Center. Please email ASXLregistry@cchmc.org