Platelet dysfunction, familial (with AML)

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

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