GRHL3 - van der Woude syndrome 2

This test is available for the following conditions:

  • Conditions > Multiple congenital anomalies (MCA) > van der Woude syndrome 2

This product is also part of the following panels:

  • Craniofacial anomalies panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Orofacial clefting 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

OMIM: 608317
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane



€ 451
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Gene

GRHL3 - van der Woude syndrome 2

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 451
View Add

GRHL3 - van der Woude syndrome 2


€ 451
Add