TSHZ1 - congenital auditory canal atresia

This test is available for the following conditions:

  • Conditions > Multiple congenital anomalies (MCA) > Congenital aural atresia (CAA)
  • Conditions > Hearing impairment > Congenital aural atresia (CAA)

This product is also part of the following panels:

  • Craniofacial anomalies panel with genome wide CNV analysis
  • Hearing impairment panel (including GJB2)
  • Mendelian inherited disorders panel with genome wide CNV analysis

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 607842
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane



€ 369
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Gene

TSHZ1 - congenital auditory canal atresia

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 369
View Add

TSHZ1 - congenital auditory canal atresia


€ 369
Add