Peutz-Jeghers syndrome

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 hereditary colorectal and polyposis
• Panel hereditary pancreatic cancer (BRCA1, BRCA2, PALB2, ATM, CDKN2A, MLH1, MSH2, MSH6, PMS2, STK11)
• 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

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