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Stories brought to you by CUL3 Support & Awareness and the families of those living with CUL3-related neurodevelopmental disorder.

September 2023 2 posts
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Amanda N

May 19, 2023

Children's Books Celebrating Diversity and Inclusion

Children's Books Celebrating Diversity and Inclusion

Amanda N

May 13, 2023

Donating Blood or Tissue Samples to Support Research on Rare Diseases

Donating Blood or Tissue Samples to Support Research on Rare Diseases

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DISCLAIMER: The information on this website has been developed by parents of children with a CUL3-related genetic diagnosis and is not intended to replace information provided to you by a healthcare provider. Always consult a licensed medical professional with questions or concerns regarding a medical condition.

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