TBX5 - Holt-Oram syndrome ¹
This test is available for the following conditions:
- Conditions > Cardiovascular > Holt-Oram syndrome
This product is also part of the following panels:
- WES congenital heartdisease ¹ (% *)
- WES heart disorders¹ (% *)
- WES Mendelian inherited disorders (% *)
- WES short stature/skeletal dysplasia (% *)
* % 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
- Deletion/duplication analysis (MLPA)
OMIM:
601620
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane