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Craniosynostosis syndromes (Apert, Crouzon)
FGFR2
Crouzon syndrome
,
Apert syndrome
Centrum Medische Genetica - UZ Antwerpen
Craniosynostosis / Apert syndrome (hot spot mutations - exon 7)
FGFR2
Apert syndrome
Centre de Génétique Humaine - CHU Sart-Tilman
Familial hemiplegic Migraine (gene panel)
Familial hemiplegic Migraine (8 genes) - KUL
Familial or sporadic hemiplegic migraine
Centrum Menselijke Erfelijkheid - KUL
Sessile serrated polyposis syndrome (RNF43 gene)
RNF43
Serrated polyposis syndrome
Centre de Génétique Humaine - CHU Sart-Tilman
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