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FOXG1 Research Foundation

About
What is FOXG1 Syndrome?
Our Story
Our Mission
Our Team
Our Partners
Australia Chapter
We Remember
Contact Us
News / Blog
Research
Research & Development
Scientific Advisory Board
Path to a Cure
FOXG1 Science Team
Research Assets & Grants
FOXG1 Key Papers
Parents & Caregivers
Newly Diagnosed
Resources
FOXG1 Ciitizen Natural History Study
Patient Data Center | Registry
Stem Cell Biobank
Brain Donation
Clinical Centers
FOXG1 Amazon Store
Events
2024 FOXG1 Conference
Citizen Natural History Study
FOXG1 Store
2024 RACE TO $250K TEAMS
GET INVOLVED
Donate
January Newsletter: Big Things in 2019
January 31, 2019
Blog Post
Nicole Johnson
January Newsletter: Big Things in 2019
Nicole Johnson
January 31, 2019
Blog Post

January Newsletter: Big Things in 2019

Nicole Johnson
January 31, 2019
Blog Post

View the Full Newsletter in your bowser HERE

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https://www.foxg1research.org/foxg1-patient-registry/

https://www.foxg1research.org/foxg1-patient-registry/

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www.foxg1research.org/donate

www.foxg1research.org/donate

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www.foxg1research.org

www.foxg1research.org

Tagged: foxg1 syndrome, research update, science, FOXG1 syndrome

Newer PostThe FOXG1 Research Foundation Announces the Launch of its Global Patient Registry to Accelerate Research For the Rare Genetic Disease, FOXG1 Syndrome
Older PostThe First FOXG1 Scientists Symposium - A Recap.
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