MYH9 - Fechtner syndrome

This test is available for the following conditions:

  • Conditions > Hematological, hereditary > Fechtner 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




€ 641

Gene

MYH9 - Fechtner syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 641

MYH9 - Fechtner syndrome



€ 641