HNF1B - autosomal dominant renal cysts and diabetes syndrome
This test is available for the following conditions:
- Conditions > Renal / Nephrological > Renal cysts and diabetes syndrome
This product is also part of the following panels:
- Liver disorders panel
- Mendelian inherited disorders panel with genome wide CNV analysis
- Renal disorders panel
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