SLC26A2 - achondrogenesis, type 1B ¹

This test is available for the following conditions:

  • Conditions > Skeletal > Achondrogenesis

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
  • Orofacial clefting panel with genome wide CNV analysis
  • Short stature/skeletal dysplasia panel with genome wide CNV analysis
  • 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: 606718
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane



€ 410
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Gene

SLC26A2 - achondrogenesis, type 1B ¹

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Maastricht UMC+
€ 410
View Add

SLC26A2 - achondrogenesis, type 1B ¹


€ 410
Add