FAM20A - amelogenesis imperfecta type IG (enamel-renaal syndroom)

This test is available for the following conditions:

  • Conditions > Renal / Nephrological > Amelogenesis imperfecta

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Craniofacial anomalies panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Renal disorders panel
  • 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: 611062
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane



€ 402
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Gene

FAM20A - amelogenesis imperfecta type IG (enamel-renaal syndroom)

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 402
View Add

FAM20A - amelogenesis imperfecta type IG (enamel-renaal syndroom)


€ 402
Add