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Sciensano
Test Cytogenetics analysis (BCR-ABL fusion gene ((t(9;22)) / Philadelphia chromosome)
Sciensano
Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 et 21 and sex chromosomes
Chromosome 21
,
Chromosome 13
,
Chromosome 18
Down syndrome
,
Trisomy 13
,
Trisomy 18
Centrum Menselijke Erfelijkheid - KUL
Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 et 21 and sex chromosomes
Chromosome 21
,
Chromosome 13
,
Chromosome 18
Down syndrome
,
Trisomy 13
,
Trisomy 18
Centrum Medische Genetica - UZ Gent
Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 et 21 and sex chromosomes
Chromosome 21
,
Chromosome 13
,
Chromosome 18
Down syndrome
,
Trisomy 13
,
Trisomy 18
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 et 21 and sex chromosomes
Chromosome 21
,
Chromosome 13
,
Chromosome 18
Centrum Medische Genetica - UZ Brussel VUB
Corneal dystrophy (gene panel)
Corneal dystrophy - UGent
Centrum Medische Genetica - UZ Gent
Intellectual disability (virtual gene panel)
Intellectual disability (gene panel)
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
Hereditary Spastic Paraplegia (gene panel)
Hereditary Spastic Paraplegia & ataxia (genepanel) - UZA
Centrum Medische Genetica - UZ Antwerpen
Myopathy (gene panel)
Myopathy (genepanel) - UZA
Centrum Medische Genetica - UZ Antwerpen
Peripheral neuropathy (gene panel)
Neuropathy (genepanel) - UZA
Centrum Medische Genetica - UZ Antwerpen
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
Amyotrophic Lateral Sclerosis (ALS) (gene panel)
Amyotrophic Lateral Sclerosis (ALS) - UGent
Amyotrophic lateral sclerosis
,
Juvenile amyotrophic lateral sclerosis
,
Amyotrophic lateral sclerosis type 4
Centrum Medische Genetica - UZ Gent
Pediatric oncopredisposition (gene panel)
Pediatric oncopredisposition - UGent
Centrum Medische Genetica - UZ Gent
Endocrine Disorders - Hypothyroidism (gene panel - 42 genes)
Endocrine Disorders - Hypothyroidism (42 genes) - ULB
Centre de Génétique Humaine - Erasme ULB
Endocrine Disorders - Hyper(Hypo)parathyroidism (gene panel - 24 genes)
Endocrine Disorders - Hyper(Hypo)parathyroidism (24 genes) - ULB
Centre de Génétique Humaine - Erasme ULB
Telomeropathies (virtual gene panel)
Centre de Génétique Médicale UCL
Hepatology (gene panel)
Hepatology panel - UGent
Centrum Medische Genetica - UZ Gent
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