SH3PXD2B - Frank-Ter Haar syndrome

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Frank-Ter Haar syndrome
  • Conditions > Multiple congenital anomalies (MCA) > Frank-Ter Haar syndrome

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Short stature/skeletal dysplasia panel with genome wide CNV analysis
  • Vision disorders panel

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

Method

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

OMIM: 249420
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 435

Gene

SH3PXD2B - Frank-Ter Haar syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 435

SH3PXD2B - Frank-Ter Haar syndrome



€ 435