Orphanet: Molecular Diagnosis of Hereditary Renal Cancer NGS Panel 16 genes
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Molecular Diagnosis of Hereditary Renal Cancer - NGS Panel (16 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: February 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

Additional information

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.