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GPSM2 - Chudley-McCullough syndrome

This test is available for the following conditions:

Conditions > Hearing impairment > Chudley-McCullough syndrome
Conditions > Skeletal > Chudley-McCullough syndrome

This product is also part of the following panels:

Comprehensive preconception carrier test panel¹
Hearing impairment panel (including GJB2)
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: 609245
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

GEN

complete analysis

targeted analysis of a familial mutation

€ 443

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Chudley-McCullough syndrome

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Gene

GPSM2 - Chudley-McCullough syndrome

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Performing laboratory
Radboudumc

€ 443

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GPSM2 - Chudley-McCullough syndrome

GEN

complete analysis

targeted analysis of a familial mutation

€ 443

Add Update Remove

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