FGF9 - multiple synostoses syndrome

This test is available for the following conditions:

  • Conditions > Hearing impairment > Multiple synostosis syndrome
  • Conditions > Skeletal > Multiple synostosis syndrome

This product is also part of the following panels:

  • Craniofacial anomalies panel
  • Mendelian inherited disorders panel
  • Short stature/skeletal dysplasia panel

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

Method

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

OMIM: 600921
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 336

Gene

FGF9 - multiple synostoses syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 336

FGF9 - multiple synostoses syndrome



€ 336
Gene

GDF5 - multiple synostoses syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 369

GDF5 - multiple synostoses syndrome



€ 369

GDF5 - multiple synostoses syndrome

This test is available for the following conditions:

  • Conditions > Hearing impairment > Multiple synostosis syndrome
  • Conditions > Skeletal > Multiple synostosis syndrome

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders panel
  • Short stature/skeletal dysplasia panel
  • 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: 601146
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 369
Gene

NOG - multiple synostoses syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 327

NOG - multiple synostoses syndrome



€ 327

NOG - multiple synostoses syndrome

This test is available for the following conditions:

  • Conditions > Hearing impairment > Multiple synostosis syndrome
  • Conditions > Skeletal > Multiple synostosis syndrome

This product is also part of the following panels:

  • Craniofacial anomalies panel
  • Hearing impairment panel (including GJB2)
  • Mendelian inherited disorders panel
  • Short stature/skeletal dysplasia panel

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

Method

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

OMIM: 602991
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 327