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HNF1B - congenital anomalies of the kidney and urinary tract

This test is available for the following conditions:

Conditions > Renal / Nephrological > Cong. anomalies of kidney/urinary tract (CAKUT)

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: 189907
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane

GEN

complete analysis

targeted analysis of a familial mutation

€ 665

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Cong. anomalies of kidney/urinary tract (CAKUT)

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