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Disease
Laboratory
Intellectual disability (virtual gene panel)
Intellectual disability (gene panel)
Centre de Génétique Médicale UCL
Telomeropathies (virtual gene panel)
Centre de Génétique Médicale UCL
Epileptic encephalopathies (virtual gene panel)
Centre de Génétique Médicale UCL
Rasopathies (virtual gene panel)
Centre de Génétique Médicale UCL
Whole exome sequencing
Centre de Génétique Médicale UCL
cleft lip with/whitout cleft palate (virtual gene panel)
Cleft lip and palate / dysmorphic facial features / craniofacial anomalies (255 genes)) - UCL
Cleft lip/palate
Centre de Génétique Médicale UCL
Osteogenesis Imperfecta (gene panel)
Osteogenesis Imperfecta (25 genes) - KUL
Centrum Menselijke Erfelijkheid - KUL
Stickler syndrome (gene panel)
Stickler (6 genes) - KUL
Centrum Menselijke Erfelijkheid - KUL
Craniosynostosis (gene panel)
Craniosynostosis (32 genes) - KUL
Centrum Menselijke Erfelijkheid - KUL
Dystonia (gene panel)
Dystonia (68 genes) - KUL
Centrum Menselijke Erfelijkheid - KUL
Skeletal Dysplasia (gene panel)
Centrum Menselijke Erfelijkheid - KUL
Developmental disorders: intellectual disability and multiple congenital anomalies (gene panel)
Developmental disorders: intellectual disability and multiple congenital anomalies (gene panel) - KUL
Centrum Menselijke Erfelijkheid - KUL
Genetic disorders of Calcium and Phosphate metabolism (gene panel)
Genetic disorders of Calcium and Phosphate metabolism (31 genes) - KUL
Centrum Menselijke Erfelijkheid - KUL
Inherited Kidney Diseases (Gene Panel)
Panel Nephro-ULG-V1
Centre de Génétique Humaine - CHU Sart-Tilman
Congenital structural heart defects (gene panel)
Congenital structural heart defects - UGent
Centrum Medische Genetica - UZ Gent
Neurodegeneration with Brain Iron Accumulation (gene panel)
Neurodegeneration with Brain Iron Accumulation (NBIA) - UGent
Centrum Medische Genetica - UZ Gent
Nephrogenetics / Nephropathy (gene panel)
Nephropathy panel - UGent
Centrum Medische Genetica - UZ Gent
Disorders of sex development - Primary Ovarian insufficiency - Hypogonadotropic Hypogonadism (gene panel)
Disorders of Sex Development - Primary Ovarian Insufficiency - Hypogonadotropic Hypogonadism - UGent
Centrum Medische Genetica - UZ Gent
Microphthalmia / Anophthalmia / Coloboma-Anterior Segment Dysgenesis (MAC-ASD) (gene panel)
Microphthalmia/Anophthalmia/Coloboma - Anterior Segment Dysgenesis - UGent
Centrum Medische Genetica - UZ Gent
Movement Disorders (gene panel)
Movement Disorders - UGent
Centrum Medische Genetica - UZ Gent
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