MID1 - Opitz G/BBB syndrome

This test is available for the following conditions:

  • Conditions > Multiple congenital anomalies (MCA) > Opitz G/BBB syndrome

This product is also part of the following panels:

  • WES craniofacial anomalies (% *)
  • WES intellectual disability (% *)
  • WES Mendelian inherited disorders (% *)
  • WES orofacial clefting (% *)

* % 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: 300000
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 674

Gene

MID1 - Opitz G/BBB syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Radboudumc
€ 674

MID1 - Opitz G/BBB syndrome



€ 674