MYH9 - Epstein syndrome
This test is available for the following conditions:
- Conditions > Hematological, hereditary > Epstein 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
- Sequence analysis of all coding exons and flanking intron-exon boundaries
OMIM:
160775
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane