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Wiskott-Aldrich syndrome
WAS
Wiskott-Aldrich syndrome
Centrum Menselijke Erfelijkheid - KUL
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
Pseudoxanthoma Elasticum
Pseudoxanthoma Elasticum - UGent
Pseudoxanthoma elasticum
Centrum Medische Genetica - UZ Gent
Hypocalciuric hypercalcemia, familial type II
GNA11
Familial hypocalciuric hypercalcemia type 2
Centre de Génétique Humaine - CHU Sart-Tilman
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