ESCO2 - Roberts syndrome

This test is available for the following conditions:

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

This product is also part of the following panels:

  • WES comprehensive preconception carrier test ¹
  • WES intellectual disability (97.3% **)
  • WES Mendelian inherited disorders (97.3% **)
  • WES short stature/skeletal dysplasia (97.3% **)

** % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

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

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 609353
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 418

Gene

ESCO2 - Roberts syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 418

ESCO2 - Roberts syndrome



€ 418