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Get the free AUTISM GENETIC RESOURCE EXCHANGE (AGRE) - tourette-repository

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New Jersey Center for Tourette Syndrome Sharing Repository (NJ CTS Sharing Repository) Funded by New Jersey Center for Tourette Syndrome and Associated Disorders (NJ CTS) NJ CTS SHARING REPOSITORY
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01
Go to the Autism Genetic Resource Exchange website.
02
Click on the 'Registration' button.
03
Fill out the required information such as your name, email, and contact details.
04
Verify your email address by clicking on the confirmation link sent to your email.
05
Login to your account using the provided credentials.
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Navigate to the 'Fill Out Form' section.
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Complete the required fields in the form related to the autism genetic resource exchange.
08
Upload any necessary documents or genetic data as specified.
09
Review all the information provided for accuracy.
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Submit the completed form.
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Wait for confirmation or further instructions from the Autism Genetic Resource Exchange team.

Who needs autism genetic resource exchange?

01
Researchers studying autism and its genetic basis.
02
Clinicians and medical professionals involved in diagnosing and treating individuals with autism.
03
Families and individuals affected by autism who wish to contribute their genetic information to advance research and understanding of the condition.
04
Scientists and geneticists exploring the genetic factors associated with autism spectrum disorders.
05
Organizations and institutions dedicated to autism research and advocacy.
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Autism Genetic Resource Exchange (AGRE) is a program that collects and shares genetic samples and clinical data from families affected by autism.
Researchers and clinicians studying autism spectrum disorders are required to file autism genetic resource exchange.
To fill out autism genetic resource exchange, researchers and clinicians can visit the AGRE website and follow the instructions for submitting genetic samples and clinical data.
The purpose of autism genetic resource exchange is to facilitate research on the genetic causes of autism spectrum disorders and improve understanding and treatment of the condition.
Information such as genetic samples, clinical data, family medical history, and demographic information must be reported on autism genetic resource exchange.
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