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LMBR1 - polysyndactyly

This test is available for the following conditions:

Conditions > Multiple congenital anomalies (MCA) > Polysyndactyly
Conditions > Skeletal > Polysyndactyly

This product is also part of the following panels:

Comprehensive preconception carrier test panel¹
Mendelian inherited disorders panel with genome wide CNV analysis
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
Deletion/duplication analysis (MLPA)

OMIM: 605522
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

GEN

complete analysis

targeted analysis of a familial mutation

€ 451

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- Radboudumc & MaasrichtUMC+

Polysyndactyly

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Gene

LMBR1 - polysyndactyly

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

Performing laboratory
Radboudumc

€ 451

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LMBR1 - polysyndactyly

GEN

complete analysis

targeted analysis of a familial mutation

€ 451

Add Update Remove

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