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Molecular Syndromology|July 14, 2026
Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos SyndromeSabri Aynacı, Sinem Kocagil, Oğuz ÇilingirMolecular Syndromology|May 15, 2026
IFT43-Related Cranioectodermal Dysplasia Type 3: Clinical and Molecular Insights from the First Reported Turkish PatientSinem Kocagil, Hilal Gölcür, Sabri Aynacı, et al.Molecular Syndromology|May 7, 2025
A Novel de novo Exceptional Complex Chromosomal Rearrangement Involving 5 Chromosomes Resulting in Neurodevelopmental Delay and DysmorphismSabri Aynacı, Sinem Kocagil, Coşkun Yarar, et al.Pageof 1