FGFR3 - hypochondroplasia ¹

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Hypochondroplasia

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
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Gene

FGFR3 - hypochondroplasia ¹

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

FGFR3 - hypochondroplasia ¹


€ 484
Add