TFAP2A - branchio-oculo-facial syndrome

This test is available for the following conditions:

  • Conditions > Multiple congenital anomalies (MCA) > Branchio-oculo-facio syndrome (BOF)
  • Conditions > Hearing impairment > Branchio-oculo-facio syndrome (BOF)
  • Conditions > Vision impairment / blindness > Branchio-oculo-facio syndrome (BOF)

This product is also part of the following panels:

  • WES craniofacial anomalies (98.0% **)
  • WES intellectual disability (98.0% **)
  • WES Mendelian inherited disorders (98.0% **)
  • WES skin disorders¹ (98.0% **)

** % 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: 113620
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 386

Gene

TFAP2A - branchio-oculo-facial syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 386

TFAP2A - branchio-oculo-facial syndrome



€ 386