Schinzel-Giedion syndrome

SETBP1 - Schinzel-Giedion syndrome

This test is available for the following conditions:

• Conditions > Multiple congenital anomalies (MCA) > Schinzel-Giedion syndrome

This product is also part of the following panels:

• Intellectual disability panel with genome wide CNV analysis
• Mendelian inherited disorders 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: 269150
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

---