FLCN - Birt-Hogg-Dubé syndrome ¹

This test is available for the following conditions:

  • Conditions > Skin > Birt-Hogg-Dubé syndrome

This product is also part of the following panels:

  • Hereditary cancer panel
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • panel hereditary renalcancer (SDHA, SDHB, SDHC, SDHD, SDHAF2, VHL, PTEN, FLCN, MET, FH, BAP1)
  • Skin disorders panel¹

Turnaround time
Complete analysis: 6 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
  • Deletion/duplication analysis (MLPA)

OMIM: 607273
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 476

Gene

FLCN - Birt-Hogg-Dubé syndrome ¹

Turnaround time
Complete analysis: 6 weeks / Targeted analysis: 4 weeks
Performing laboratory
Maastricht UMC+
€ 476

FLCN - Birt-Hogg-Dubé syndrome ¹



€ 476