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Welcome to the 17q12 Interest Group registry page! The purpose of this registry is to gain a better understanding of the medical, developmental, and behavioral features associated with 17q12 deletions and duplications.

The information provided by individuals and their families will help improve the diagnosis and clinical care for all those affected by this rare genetic variant. The information that you provide is “de-identified” by Patient Crossroads, meaning no one will be able to see your name, date of birth, or other identifying data.

Please take a moment to register- your participation is invaluable in advancing our knowledge of 17q12 deletions and duplications and improving the lives of affected individuals and their families.

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Our Mission

As researchers and clinical care providers at Geisinger’s Autism & Developmental Medicine Institute, our mission with this registry is to advance knowledge about 17q12 deletions and duplications. Our hope is that such knowledge will drive medical and behavioral interventions and improve outcomes for individuals who have been diagnosed. We also hope that this registry will serve to unite people from around the world while empowering patients and their families to connect and provide support to each other.

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