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ZEB2 - Mowat-Wilson syndrome

This test is available for the following conditions:

Conditions > Intellectual Disability > Mowat-Wilson syndrome
Conditions > Multiple congenital anomalies (MCA) > Mowat-Wilson syndrome

This product is also part of the following panels:

Craniofacial anomalies panel with genome wide CNV analysis
Epilepsy panel
Intellectual disability panel with genome wide CNV analysis
Mendelian inherited disorders panel with genome wide CNV analysis
Orofacial clefting 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

Remarks
MLPA analysis for this gene will not be performed routinely. Deletions can be detected with high resolution SNP array and can be requested seperately.

OMIM: 235730
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

GEN

complete analysis

targeted analysis of a familial mutation

€ 410

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