ANKRD11 - KBG syndrome
This test is available for the following conditions:
- Conditions > Intellectual Disability > KBG syndrome
- Conditions > Multiple congenital anomalies (MCA) > KBG syndrome
This product is also part of the following panels:
- Congenital heartdisease panel¹
- Craniofacial anomalies panel
- Epilepsy panel
- Heart disorders panel¹
- Intellectual disability panel
- Mendelian inherited disorders panel
- Orofacial clefting panel
- Short stature/skeletal dysplasia panel
- Skin disorders panel¹
Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
611192
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane