Skip to main content
Log in
Sciensano
Support
Toggle navigation
Main navigation
Home
Genetic tests
Analytes
Diseases
Labs
Guide
Contact
Genetic tests
20
50
100
Search
Reset
Full name
Analytes
Gene panels
Disease
Laboratory
chronic progressive external o
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
Centrum Medische Genetica - UZ Brussel VUB
facioscapulohumeral muscular d
FRG1
Facioscapulohumeral dystrophy
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
fragile syndrome and fragile x
FMR1
Fragile X syndrome
,
Fragile X-associated tremor/ataxia syndrome
,
Symptomatic form of fragile X syndrome in female carriers
Centre de Génétique Humaine - CHU Sart-Tilman
fragile syndrome pof fxtas cgg
FMR1
Fragile X syndrome
,
Fragile X-associated tremor/ataxia syndrome
,
Symptomatic form of fragile X syndrome in female carriers
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
fukuyama congenital muscular d
FKTN
Congenital muscular dystrophy, Fukuyama type
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
myoclonic epilepsy unverricht
CSTB
Progressive myoclonic epilepsy type 1
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
steinert myotonic dystrophy ct
DMPK
Steinert myotonic dystrophy
Centrum Menselijke Erfelijkheid - KUL
steinert myotonic dystrophy ct
DMPK
Steinert myotonic dystrophy
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
steinert myotonic dystrophy dm
DMPK
Steinert myotonic dystrophy
Centrum Medische Genetica - UZ Brussel VUB
Did not find what you were looking for? Contact us through the support center.
Read more