FGFR3 - thanatofore dysplasia ¹

This test is available for the following conditions:

  • Conditions > Skeletal > Thanatofore dysplasia

This product is also part of the following panels:

  • WES craniofacial anomalies (% *)
  • WES hearing impairment (including GJB2) (% *)
  • WES intellectual disability (% *)
  • WES Mendelian inherited disorders (% *)
  • WES short stature/skeletal dysplasia (% *)
  • WES skin disorders¹ (% *)

* % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

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

Method

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

OMIM: 134934
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 484

Gene

FGFR3 - thanatofore dysplasia ¹

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Maastricht UMC+
€ 484

FGFR3 - thanatofore dysplasia ¹



€ 484