MED12 - Lujan-Fryns syndrome

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Lujan-Fryns syndrome
  • Conditions > Multiple congenital anomalies (MCA) > Lujan-Fryns syndrome

This product is also part of the following panels:

  • WES craniofacial anomalies (95.5% **)
  • WES epilepsy (95.5% **)
  • WES intellectual disability (95.5% **)
  • WES Mendelian inherited disorders (95.5% **)
  • WES skin disorders¹ (95.5% **)

** % 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: 309520
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 558

Gene

MED12 - Lujan-Fryns syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 558

MED12 - Lujan-Fryns syndrome



€ 558