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:

  • Craniofacial anomalies panel with genome wide CNV analysis
  • Hearing impairment panel (including GJB2)
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Short stature/skeletal dysplasia panel with genome wide CNV analysis
  • Skin disorders panel¹
  • Tall stature panel with genome wide CNV analysis

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