SYNGAP1 - autosomal dominant intellectual disability type 5

This test is available for the following conditions:

• Conditions > Multiple congenital anomalies (MCA) > Intellectual disability, autosomal dominant

This product is also part of the following panels:

• Epilepsy panel
• Intellectual disability / developmental delay panel with genome wide CNV analysis
• Mendelian inherited disorders panel with genome wide CNV analysis

Turnaround time
Complete analysis & Targeted analysis: 12 weeks

Method

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

OMIM: 612621
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

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