FGB - Dysfibrinogenemia

This test is available for the following conditions:

  • Conditions > Hematological, hereditary > Fibrinogenemia (a-, hypo-, dys-)

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Hemostatic/thrombotic disorders panel
  • Mendelian inherited 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: 134830
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 378

Gene

FGA - Dysfibrinogenemia

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 386

FGA - Dysfibrinogenemia



€ 386

FGA - Dysfibrinogenemia

This test is available for the following conditions:

  • Conditions > Hematological, hereditary > Fibrinogenemia (a-, hypo-, dys-)

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Hemostatic/thrombotic disorders panel
  • Mendelian inherited 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: 134820
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 386
Gene

FGB - Dysfibrinogenemia

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 378

FGB - Dysfibrinogenemia



€ 378
Gene

FGG - Dysfibrinogenemia

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 378

FGG - Dysfibrinogenemia



€ 378

FGG - Dysfibrinogenemia

This test is available for the following conditions:

  • Conditions > Hematological, hereditary > Fibrinogenemia (a-, hypo-, dys-)

This product is also part of the following panels:

  • Comprehensive preconception carrier test panel¹
  • Hemostatic/thrombotic disorders panel
  • Mendelian inherited 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: 134850
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 378