Wilms tumor (DICER1; WT1 genes)

Genetic test Export to PDF

Full name:	Wilms tumor (DICER1; WT1 genes)
Test type:	Clinical
Test specialty:	Molecular Genetics
Test purpose:	Post-natal Diagnosis
Specimen:	Peripheral (whole) blood on EDTA
Method category:	Sequence analysis: entire coding region Deletion/duplication analysis
Method technique:	Next Generation Sequencing (NGS)
Laboratory:	Centrum Menselijke Erfelijkheid - KUL
RIZIV code:	565530-565541
Accreditation (ISO 15189):	2021-07-08 / 2026-02-02
Turnaround time (maximum):	4 - 6 months
Document(s):	Request form (20210603) - KUL.pdf626.4 KB
Created:	23 Jul 2019 - 15:25
Changed:	01 Mar 2023 - 16:11
URL:	https://laboboeken.nexuzhealth.com/pboek/internet/GHB%20CME/13400

Related Diseases

• Frasier syndrome
• Meacham syndrome
• Nephroblastoma

Related Laboratories

• Centrum Menselijke Erfelijkheid - KUL

Related Analytes

• DICER1
• WT1

Related Gene Panels

• Wilms' tumor (2 genes) - KUL
  Details

  Gene	% of coding sequence sufficiently covered to detect heterozygous mutations	Copy number variation	Comments
  DICER1	100.00	1
  WT1	100.00	1