The NR2F1 Foundation is making history with the launch of the first BBSOAS Center of Excellence at Cincinnati Children’s Hospital on April 21, 2023. The BBSOAS Center of Excellence, led...
Posted by | January 6, 2023
The NR2F1 Foundation had a tremendous year of achievements in 2022, so as the year has come to a close, we look back and reflect on all that has happened during...
Posted by | December 7, 2022
One of the primary objectives of the NR2F1 Foundation has been the expansion of our global research network for BBSOAS research. We will provide initial funds for a project called...
Posted by | November 18, 2021
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Posted by | November 18, 2021
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Posted by | November 18, 2021
Click the image to watch the video. Meet Zeb from the Netherlands, a young man who lives with a very rare NR2F1 disease caused by a NR2F1 gene variant, Bosch-Boonstra-Schaaf...
Posted by | November 18, 2021
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Posted by | November 18, 2021
Mom, Cecilia shares with us all about Simon. Cuantos años tiene Simón, y cómo escogieron su nombre? How old is Simón and how did you choose his name? Simón tiene 4 años...
Posted by | November 18, 2021
Mom Ashlee shares with us all about Emma. How did you choose the name Emma? Her first name was chosen before we even started the process to have her. Emma...
Posted by | November 18, 2021
Angélique shares with us all about Charly from Lyon, France. (Translated into English by Carlie Monnier) Comment avez-vous choisi le prénom de Charly? (How did you choose the name Charly?)...
