Simons Searchlight
120 Hamm Dr,
Suite 2A
Lewisburg, PA, USA
855-329-5638
About Simons Searchlight
Simons Searchlight is an online international research program for over 175 rare genetic neurodevelopmental disorders. By joining their community and sharing your experiences, you contribute to a growing database that scientists worldwide use to advance the understanding of these conditions. Through online surveys responses and optional blood collection, they gather valuable information to improve lives and drive scientific progress. Join them in shaping the future of rare genetic neurodevelopmental disorder research. Visit their website to learn more. For inquiries and questions about participation, contact their dedicated Simons Searchlight team at [email protected] .
Related Rare Diseases:
- CTNNB1 Syndrome
- Síndrome CTNNB1
- ASXL3-Related Disorder
- HNRNPU-Related Disorder
- TANC2-Related Disorders
- Trastornos relacionados con TANC2
- Trastorno relacionado a HNRNPU
- SETD1B-Related Neurodevelopmental Disorder
- SYNCRIP-Related Neurodevelopmental Disorder
- IQSEC2-Related Disorder
- Trastorno relacionado con IQSEC2
- Trastorno del neurodesarrollo relacionado con SYNCRIP
- Cohen-Gibson Syndrome
- GNB1-Related Disorder
- TLK2-Related Neurodevelopmental Disorder
- Trastorno del neurodesarrollo relacionado con TLK2
- Trastorno relacionado con GNB1
- Síndrome de Cohen-Gibson