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TGFB1 - Camurati-Engelmann disease

This test is available for the following conditions:

Conditions > Skeletal > Camurati-Engelmann disease

This product is also part of the following panels:

Comprehensive preconception carrier test panel¹
Mendelian inherited disorders panel with genome wide CNV analysis
Primary immunodeficiencies panel
Short stature/skeletal dysplasia 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: 190180
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

GEN

complete analysis

targeted analysis of a familial mutation

€ 368

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Camurati-Engelmann disease

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Gene

TGFB1 - Camurati-Engelmann disease

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

Performing laboratory
Radboudumc

€ 368

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TGFB1 - Camurati-Engelmann disease

GEN

complete analysis

targeted analysis of a familial mutation

€ 368

Add Update Remove

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