RUNX1 - familial platelet dysfunction with predisposition for AML

This test is available for the following conditions:

  • Conditions > Hematological, hereditary > Platelet dysfunction, familial (with AML)
  • Conditions > Oncogenetics > Platelet dysfunction, familial (with AML)

This product is also part of the following panels:

  • Hemostatic/thrombotic disorders panel
  • Hereditary cancer panel
  • Inherited bone marrow failure and/or predisposition panel to hematological malignancies
  • Mendelian inherited disorders panel with genome wide CNV analysis

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

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
  • Deletion/duplication analysis (MLPA)

OMIM: 151385
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane



€ 674
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Gene

RUNX1 - familial platelet dysfunction with predisposition for AML

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 674
View Add

RUNX1 - familial platelet dysfunction with predisposition for AML


€ 674
Add