Gray platelet syndrome

GFI1B - bleeding disorder, platelet-type, 17

This test is available for the following conditions:

• Conditions > Hematological, hereditary > Gray platelet syndrome

This product is also part of the following panels:

• Hemostatic/thrombotic disorders panel
• 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

OMIM: 604383
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

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