Orphanet: Pediatric Cancer NGS Panel 12 genes
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Pediatric Cancer NGS Panel (12 genes)

  • Calgary Molecular Diagnostic Laboratory
  • Alberta Health Services
  • Alberta Children's Hospital
  • 2888 Shaganappi Trail NW
  • T3B 6A8 CALGARY
  • CANADA
  • Director of laboratory : Dr Jillian PARBOOSINGH
  • More information
  • Phone : 1(403)955-7026
  • Additional Phone : -
  • Fax : -
Last update: May 2018

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
NGS sequencing (except WES)
Deletion / Duplication analysis
MLPA based techniques
Deletion / Duplication analysis
NGS sequencing (except WES)
Deletion / Duplication analysis
PCR based techniques
Deletion / Duplication analysis
Array based techniques

List of diseases and genes

List of diseases tested (24)
Adrenocortical carcinoma
Atypical teratoid rhabdoid tumor
Beckwith-Wiedemann syndrome due to CDKN1C mutation
Choroid plexus carcinoma
Denys-Drash syndrome
Essential thrombocythemia
Familial adenomatous polyposis
Familial multinodular goiter
Familial multiple meningioma
Familial rhabdoid tumor
Frasier syndrome
Gastric adenocarcinoma and proximal polyposis of the stomach
Hereditary breast and ovarian cancer syndrome
Li-Fraumeni syndrome
Malignant sex cord stromal tumor of ovary
Medulloblastoma with extensive nodularity
Mosaic variegated aneuploidy syndrome
Nephroblastoma
Neuroblastoma
Osteosarcoma
Papilloma of choroid plexus
Pleuropulmonary blastoma familial tumor susceptibility syndrome
Turcot syndrome with polyposis
WAGR syndrome
List of genes tested (including panels) (12)
ALK
APC
BUB1B
CDKN1C
CEP57
DICER1
PHOX2B
PTCH1
SMARCB1
SUFU
TP53
WT1
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