Orphanet: Diagnosis of arrhythmogenic right ventricular cardiomyopathie Panel
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Diagnosis of arrhythmogenic right ventricular cardiomyopathie (Panel)

  • Institüt für Medizinische Molekulargenetik
  • Universität Zürich
  • Wagistrasse 12
  • 8952 SCHLIEREN
  • SWITZERLAND
  • Director of laboratory : Pr Wolfgang BERGER
  • More information
  • Phone : 0041 (0)44 556 33 50
  • Additional Phone : -
  • Fax : 0041 (0)44 556 33 51
  • Website
  • Contact
Last update: January 2022

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
Sanger sequencing
Targeted mutation analysis
NGS sequencing (except WES)
Targeted mutation analysis
PCR based techniques
Mutation scanning/screening and sequence analysis of selected exons
Sanger sequencing
Mutation scanning/screening and sequence analysis of selected exons
NGS sequencing (except WES)
Mutation scanning/screening and sequence analysis of selected exons
PCR based techniques
Sequence analysis: entire coding region
Sanger sequencing
Sequence analysis: entire coding region
NGS sequencing (except WES)
Sequence analysis: entire coding region
Whole Exome Sequencing (WES)
Deletion / Duplication analysis
NGS sequencing (except WES)
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.