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:

  • WES craniofacial anomalies (97.1% **)
  • WES epilepsy (97.1% **)
  • WES intellectual disability (97.1% **)
  • WES Mendelian inherited disorders (97.1% **)
  • WES short stature/skeletal dysplasia (97.1% **)
  • WES skin disorders¹ (97.1% **)

** % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

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

Gene

ANKRD11 - KBG syndrome

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

ANKRD11 - KBG syndrome



€ 550