STK11 - Peutz-Jeghers syndrome
This test is available for the following conditions:
- Conditions > Oncogenetics > Peutz-Jeghers syndrome
This product is also part of the following panels:
- Hereditary cancer panel
- Mendelian inherited disorders panel with genome wide CNV analysis
- panel polyposis (APC, MUTYH, SMAD4, BMPR1A, POLE, POLD1, NTHL1, STK11, PTEN)
- Skin disorders panel¹
Turnaround time
Complete analysis & Targeted analysis: 3 weeks
Method
- Sequence analysis of all coding exons and flanking intron-exon boundaries
- Deletion/duplication analysis (MLPA)
OMIM:
602216
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA