GJB6 - Clouston syndrome

This test is available for the following conditions:

  • Conditions > Multiple congenital anomalies (MCA) > Hidrotic Ectodermal Dysplasia (Clouston)
  • Conditions > Hearing impairment > Hidrotic Ectodermal Dysplasia (Clouston)

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Craniofacial anomalies panel with genome wide CNV analysis
  • Hearing impairment panel (including GJB2)
  • Mendelian inherited disorders 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
  • Analysis of one or more specific deletions

OMIM: 604418
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane



€ 320
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Gene

GJB6 - Clouston syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 320
View Add

GJB6 - Clouston syndrome


€ 320
Add