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Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centre de Génétique Médicale UCL
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centrum Medische Genetica - UZ Gent
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centrum Medische Genetica - UZ Antwerpen
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centre de Génétique Humaine - Erasme ULB
Huntington disease - HTT gene CAG repeat expansion
HTT
Huntington disease
Centrum Medische Genetica - UZ Brussel VUB
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centre de Génétique Humaine - CHU Sart-Tilman
Huntington disease - CAG repeat expansion
HTT
Huntington disease
Centrum Menselijke Erfelijkheid - KUL
Silver-Russell syndrome
11p15.5
,
7p12.1
,
7q32.2
Silver-Russell syndrome
,
Silver-Russell syndrome due to an imprinting defect of 11p15
,
Silver-Russell syndrome due to 11p15 microduplication
Centre de Génétique Médicale UCL
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
Amyotrophic lateral sclerosis (ALS) / Frontotemporal demention (FTD) - GGGGCC repeat expansion in C9ORF72
C9ORF72
Amyotrophic lateral sclerosis type 4
,
Frontotemporal dementia with motor neuron disease
Centrum Medische Genetica - UZ Gent
Achondrogenesis / Kniest dysplasia / Hypochondrogenesis
COL2A1
Achondrogenesis type 2
,
Hypochondrogenesis
,
Kniest dysplasia
,
Multiple epiphyseal dysplasia, Beighton type
,
Spondyloepiphyseal dysplasia congenita
,
Stickler syndrome type 1
Centrum Medische Genetica - UZ Gent
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