International FOXP1 Foundation
Our mission is to build a global community that empowers and supports families and individuals with FOXP1 syndrome by sharing knowledge, inspiring hope, supporting research, and raising awareness. Our mission is to build a global community that empowers and supports families and individuals with FOXP1 syndrome by sharing knowledge, inspiring hope, encouraging research, and raising awareness.
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HOME | FOXP1 Foundation HOME FOXP1 SYNDROME RESEARCH FAMILIES ABOUT US GET INVOLVED More Advancing ResearchEmpowering Families Now Hiring Executive Director Click Here for More Information FOXP1 syndrome is a rare genetic disorder characterized by delays in early motor and language milestones mildtosevere intellectual deficits speech and language impairment and behavior abnormalities. The International FOXP1 Foundation is committed to building a global community that empowers and supports families and individuals with FOXP1 syndrome by sharing knowledge inspiring hope encouraging research and raising awareness. INFORMATION AND RESOURCES While there is still so much unknown and no real changes in our daytoday life with the diagnosis it was a relief to have an answer and explanation for everything about Joey that had felt off. It is amazing to feel the support from the other families and to know we are not alone.
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Birth Defects, Genetic Diseases Research Category
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Our mission is to advocate, educate, and raise funds for research towards SPATA5 & SPATA5L1 Disorders.
63. International FOXP1 Foundation
Our mission is to build a global community that empowers and supports families and individuals with FOXP1 syndrome by sharing knowledge, inspiring hope, supporting research, and raising awareness.
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아름다운 삶, 아름다운 마무리.
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