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Crisponi syndrome
CRLF1
Crisponi syndrome
Centre de Génétique-Institut de Pathologie et de Génétique (IPG)
Usher syndrome, type IIA
USH2A
Usher syndrome type 2
Centrum Medische Genetica - UZ Gent
Usher syndrome (gene panel)
CDH23
,
CLRN1
,
WHRN
,
ADGRV1
,
MYO7A
,
PCDH15
,
PDZD7
,
USH1C
,
USH1G
,
USH2A
Usher syndrome (10 genes) - UZA
Centrum Medische Genetica - UZ Antwerpen
Beckwith-Wiedemann syndrome (11p15 methylation)
H19
,
KCNQ1OT1
,
IGF2
Beckwith-Wiedemann syndrome due to imprinting defect of 11p15
,
Beckwith-Wiedemann syndrome
Centrum Menselijke Erfelijkheid - KUL
Familial hypercholanemia (3 genes)
BAAT
,
EPHX1
,
TJP2
Familial hypercholanemia (3 genes) - UCL
Familial hypercholanemia
Centre de Génétique Médicale UCL
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