EZH2 - Weaver syndrome

This test is available for the following conditions:

  • Conditions > Multiple congenital anomalies (MCA) > Weaver syndrome

This product is also part of the following panels:

  • Craniofacial anomalies panel with genome wide CNV analysis
  • Hereditary cancer 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
  • Short stature/skeletal dysplasia panel with genome wide CNV analysis
  • Tall stature 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: 277590
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane



€ 476
Add
Go to main content
Gene

EZH2 - Weaver syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 476
View Add

EZH2 - Weaver syndrome


€ 476
Add