Trisomy 21 Research Society (T21RS) is the first international non-profit scientific organization of researchers studying Down syndrome. T21RS was founded to promote basic and applied research on Down syndrome, stimulate translational research and apply new scientific knowledge to improve the quality of life for people with Down Syndrome.
News
“Down Syndrome: From Research to Therapy” virtual fall conference
Looking for clinical ideas, resources, or collaborators for your research?
T21RS 2021 Virtual Meeting Proceedings
COVID-19 vaccinations are safe to use in people with Down syndrome
T21RS endorses the ALBA Declaration on Equity and Inclusion
T21RS Statement with regards to vaccinations for people with Down syndrome during the COVID-19 pandemic
T21RS statement on “shielding” individuals with Down syndrome during the COVID-19 pandemic
T21RS initiatives on COVID-19
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