Delfien Syx
Gent, VLG, Belgium
Last Updated: 09/26/2026
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Found 62 publications
Next-Generation Sequencing and Variant Analysis of Fibrillar (Pro)Collagens.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: September 02, 2026
Smad3 deficiency attenuates disease severity in a zebrafish model for Smad6-related aortic disease.
Journal: Angiogenesis
Published: October 08, 2025
The Importance of Being Earnest: Putting Molecular Analysis for the Diagnosis of Pseudoxanthoma Elasticum in Perspective.
Journal: The Journal of investigative dermatology
Published: July 11, 2025
Evaluating variants of uncertain significance in adult zebrafish via prime editing: a proof of concept with a COL1A2 variant.
Journal: BMC medical genomics
Published: June 27, 2025
Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder.
Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene underlies a neurodevelopmental disorder.
Journal: medRxiv : the preprint server for health sciences
Published: August 16, 2024
Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder.
Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder.
Journal: American journal of human genetics
Published: August 09, 2024
Editorial: Ehlers-Danlos syndrome: from bedside to bench.
Journal: Frontiers in genetics
Published: March 11, 2024
Pathogenic mechanisms in genetically defined Ehlers-Danlos syndromes.
Journal: Trends in molecular medicine
Published: February 14, 2024
B3GALT6 mutations lead to compromised connective tissue biomechanics in Ehlers-Danlos syndrome.
Journal: JCI insight
Published: January 22, 2024
Analysis of matrisome expression patterns in murine and human dorsal root ganglia.
Journal: Frontiers in molecular neuroscience
Published: May 31, 2023
Last Updated: 09/26/2026