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Laugh It Up for SMS
November 22, 2014
Fort Lauderdale, FL
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November Fundraisers in the Northeast.
Who We Are
The SMS Research Foundation supports research to improve the knowledge and understanding of Smith-Magenis Syndrome.
It's your support that keeps our life-changing research programs going, and brings hope to families facing this challenge.
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Let us know who you are, share your story, or just ask a question.
Roughly 1 in 25,000 live births.
Support research to improve the knowledge and understanding of Smith-Magenis Syndrome so that viable therapeutic options can be developed to improve the quality of life of those with SMS.
Article: Retinoic acid induced-1 (Rai1) regulates craniofacial and brain development in Xenopus
Article: MBD5 haploinsufficiency is associated with sleep disturbance and disrupts circadian pathways common to Smith–Magenis and fragile X syndromes
Article: Dietary Regimens Modify Early Onset of Obesity in Mice Haploinsufficient for Rai1
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