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 with genome wide CNV analysis
  • Epilepsy panel
  • Heart disorders panel¹
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Orofacial clefting panel with genome wide CNV analysis
  • Short stature/skeletal dysplasia panel with genome wide CNV analysis
  • 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



€ 550
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Gene

ANKRD11 - KBG syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 550
View Add

ANKRD11 - KBG syndrome


€ 550
Add