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« Inherited bone marrow failures syndromes » with or without organ dysfunction
Hematologic Familiar Forms - ULG
Centre de Génétique Humaine - CHU Sart-Tilman
Hereditary Spastic Paraplegia (gene panel)
Hereditary Spastic Paraplegia & ataxia (genepanel) - UZA
Centrum Medische Genetica - UZ Antwerpen
Meningioma (gene panel)
Meningioma (3 genes) - KUL
Centrum Menselijke Erfelijkheid - KUL
Endocrine Disorders - Hyper(Hypo)parathyroidism (gene panel - 24 genes)
Endocrine Disorders - Hyper(Hypo)parathyroidism (24 genes) - ULB
Centre de Génétique Humaine - Erasme ULB
Ichthyosis (gene panel)
Ichthyosis and erythroderma (98 genes) - KUL
Centrum Menselijke Erfelijkheid - KUL
Hereditary cancer panel (gene panel)
Hereditary Cancer Solution (35 genes) - UCL
Centre de Génétique Médicale UCL
Corneal dystrophy (gene panel)
Corneal dystrophy - UGent
Centrum Medische Genetica - UZ Gent
Arrhytmogenic cardiopathy
Arrhytmogenic cardiopathy - UGent
Centrum Medische Genetica - UZ Gent
Intellectual disability (virtual gene panel)
Intellectual disability (gene panel)
Centre de Génétique Médicale UCL
Lipodystrophy and/or hyperinsulinism (gene panel)
Lipodystrophy and/or hyperinsulinism (30 genes) - IPG
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Osteogenesis Imperfecta (gene panel)
Osteogenesis Imperfecta (25 genes) - KUL
Centrum Menselijke Erfelijkheid - KUL
Myopathy (gene panel)
Myopathy (genepanel) - UZA
Centrum Medische Genetica - UZ Antwerpen
Peripheral neuropathy (gene panel)
Neuropathy (genepanel) - UZA
Centrum Medische Genetica - UZ Antwerpen
Skeletal Dysplasia (gene panel)
Centrum Menselijke Erfelijkheid - KUL
Child Interstitial Lung Disease (child - gene panel)
chILD (34 genes) - KUL
Centrum Menselijke Erfelijkheid - KUL
Primary ciliary dyskinesia (PCD) Heterotaxyies (gene panel)
Heterotaxie PCD - UGent
Centrum Medische Genetica - UZ Gent
Skeletal dysplasia (gene panel)
Skeletal dysplasia - UGent
Centrum Medische Genetica - UZ Gent
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Sciensano
Supravalvular aortic stenosis
ELN
Centrum Medische Genetica - UZ Gent
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