Publication & Citation Trends
Publications
0 total
Prolonged Right Ventricular Ejection Delay in Brugada Syndrome Depends on the Type of SCN5A Variant - Electromechanical Coupling Through Tissue Velocity Imaging as a Bridge Between Genotyping and Phenotyping. OA
Cited by 7
Semantic Scholar
Genetic Defects in TAPT1 Disrupt Ciliogenesis and Cause a Complex Lethal Osteochondrodysplasia. OA
Cited by 44
Semantic Scholar
Comprehensive evaluation of the FBN1, LTBP2 and ADAMTSL4 genes in 667 patients with ectopia lentis
Cited by 0
Semantic Scholar
Defects in TAPT1, involved in axial skeletal patterning, cause a complex lethal recessive disorder of skeletal development
Cited by 0
Semantic Scholar
P-036: Recognize the clinical picture: chronic recurrent multifocal osteomyelitis (CRMO) associated with Crohn’s disease (CD): a case report OA
Cited by 0
Semantic Scholar
P-092: The course of anaemia in children with Crohn’s disease included in a prospective registry OA
Cited by 0
Semantic Scholar
New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update OA
Cited by 63
Semantic Scholar
Kinetochore KMN network gene CASC5 mutated in primary microcephaly. OA
Cited by 118
Semantic Scholar
The mutation spectrum in RECQL4 diseases OA
Cited by 222
Semantic Scholar
Research Topics
Cardiac electrophysiology and arrhythmias
(5)
RNA Research and Splicing
(4)
Cystic Fibrosis Research Advances
(3)
Connective tissue disorders research
(3)
Ion channel regulation and function
(2)
Affiliations
Vrije Universiteit Brussel
University of Antwerp
Ghent University Hospital
Antwerp University Hospital
Research Centre for Medical Genetics