PRPH2 - autosomal dominant retinitis pigmentosa type 7

This test is available for the following conditions:

  • Conditions > Vision impairment / blindness > Retinitis Pigmentosa, autosomal dominant

This product is also part of the following panels:

  • Mendelian inherited disorders 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: 179605
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 344

Gene

NRL - autosomal dominant retinitis pigmentosa type 27

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

NRL - autosomal dominant retinitis pigmentosa type 27



€ 336

NRL - autosomal dominant retinitis pigmentosa type 27

This test is available for the following conditions:

  • Conditions > Vision impairment / blindness > Retinitis Pigmentosa, autosomal dominant

This product is also part of the following panels:

  • Mendelian inherited disorders 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: 162080
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 336
Gene

PRPH2 - autosomal dominant retinitis pigmentosa type 7

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 344

PRPH2 - autosomal dominant retinitis pigmentosa type 7



€ 344
Gene

RHO - retinitis pigmentosa type 4

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 335

RHO - retinitis pigmentosa type 4



€ 335

RHO - retinitis pigmentosa type 4

This test is available for the following conditions:

  • Conditions > Vision impairment / blindness > Retinitis Pigmentosa, autosomal dominant

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders 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: 180380
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 335
Gene

RP1 - autosomal dominant retinitis pigmentosa type 1

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 451

RP1 - autosomal dominant retinitis pigmentosa type 1



€ 451

RP1 - autosomal dominant retinitis pigmentosa type 1

This test is available for the following conditions:

  • Conditions > Vision impairment / blindness > Retinitis Pigmentosa, autosomal dominant

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Mendelian inherited disorders 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: 603937
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 451