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MYH9 - Sebastian syndrome

This test is available for the following conditions:

Conditions > Hematological, hereditary > Sebastian syndrome

This product is also part of the following panels:

Hearing impairment panel (including GJB2)
Hemostatic/thrombotic disorders panel
Inherited bone marrow failure and/or predisposition panel to hematological malignancies
Intellectual disability panel with genome wide CNV analysis
Mendelian inherited disorders panel with genome wide CNV analysis
Renal disorders panel

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

Method