PTEN - Bannayan-Riley-Ruvalcaba syndrome

This test is available for the following conditions:

  • Conditions > Intellectual Disability > Bannayan-Riley-Ruvalcaba syndrome
  • Conditions > Multiple congenital anomalies (MCA) > Bannayan-Riley-Ruvalcaba syndrome
  • Conditions > Oncogenetics > Bannayan-Riley-Ruvalcaba syndrome

This product is also part of the following panels:

  • Hereditary cancer panel
  • Intellectual disability panel with genome wide CNV analysis
  • Mendelian inherited disorders panel with genome wide CNV analysis
  • Metabolic disorders panel
  • panel hereditary renalcancer (SDHA, SDHB, SDHC, SDHD, SDHAF2, VHL, PTEN, FLCN, MET, FH, BAP1)
  • panel polyposis (APC, MUTYH, SMAD4, BMPR1A, POLE, POLD1, NTHL1, STK11, PTEN)
  • Primary immunodeficiencies panel
  • 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: 601728
Performing laboratory: Radboudumc
Authorized material(s): EDTA blood, FFPE, Isolated DNA



€ 656
Add
Go to main content
Gene

PTEN - Bannayan-Riley-Ruvalcaba syndrome

Turnaround time
Complete analysis & Targeted analysis: 3 weeks
Performing laboratory
Radboudumc
€ 656
View Add

PTEN - Bannayan-Riley-Ruvalcaba syndrome


€ 656
Add