Join us for Rare Disease Day 2024 at IBG!
Rare, but not alone! We are excited to invite you to Rare Disease Day at the Izmir Biomedicine and Genome
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NEWS & EVENTS
Research on Rahman Syndrome delivers a novel tool to study the rare genetic condition
IBG Rare and Undiagnosed Diseases Platform Member Dr. Kasim Diril’s group published a study on Rahman Syndrome in FEBS Open Bio
Read MoreMeeting Announcement – Variants of Uncertain Clinical Significance (VUS) in Pediatric Neurology Practice and Suggestions for Solutions
On January 13, 2024, between 12.45-16.15, a half-day hybrid meeting titled “Variants of Uncertain Clinical Significance (VUS) in Pediatric Neurology
Read MoreRareboost External Seminar Announcement – Prof. Dr. Ahmet Özen
We are pleased to announce an upcoming seminar featuring Prof. Dr. Ahmet Özen, a leading expert in the field of
Read MoreRare and Undiagnosed Diseases Research Area Stakeholders Status and Needs Assessment Workshop
As part of the RareBoost project, “Rare and Undiagnosed Diseases Research Area Stakeholders Status and Needs Assessment Workshop” was held
Read MoreRare and Undiagnosed Diseases Research Area Stakeholders Status and Needs Assessment Workshop
Within the scope of the RareBoost ERA Chair project supported by the European Union H2020 program at Izmir Biomedicine and
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