Victor McKusick Fellows (Marfan syndrome worldwide)
The Victor McKusick Fellows program from The Marfan Foundation supports postdoctoral fellows embarking on a scientific career in biomedical research related to the rare disease…...
Research funding and funders focused on genetic disorders.
The Victor McKusick Fellows program from The Marfan Foundation supports postdoctoral fellows embarking on a scientific career in biomedical research related to the rare disease…...
The ATS/Fisher & Paykel Healthcare Research Grant in Nasal High Flow from the American Thoracic Society (ATS) is funded together Fisher & Paykel Healthcare. The…...
The Statistical Support funding program from The Ehlers-Danlos Society provides researchers worldwide working on the rare diseases Ehlers–Danlos syndromes with statistical support services. Applications are
The Medical Writer Support funding program from The Ehlers-Danlos Society provides researchers worldwide working on the rare diseases Ehlers–Danlos syndromes with access to medical writers’…...
The Open Access Funding program from The Ehlers-Danlos Society supports researchers worldwide working on the rare diseases Ehlers–Danlos syndromes. The Funding enables researchers to publish…...
The Ehlers-Danlos Society is a U.S.-based global nonprofit organization dedicated to saving and improving the lives of those affected by the Ehlers-Danlos syndromes (EDS) and
The Orphan Disease Center Million Dollar Bike Ride Pilot Grant Program is offered by The Orphan Disease Center of the University of Pennsylvania and is…...
The Project Grant funded by Action A-T support research on Ataxia-Telangiectasia that help with understanding the underlying mechanisms that lead to ataxia, developing interventions that…...
The Travel Award Supplement from the Cystic Fibrosis Foundation supports PhD students, postdoctoral fellows, and junior faculty participating in off-site training opportunities to learn new research skills…...
The Scientific Meeting Sponsorship funded by the Alpha-1 Foundation supports scientific meetings,workshops or conferences relevant to AAT Deficiency. Applications are open to rare disease researchers…...
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