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Diagnosis of epileptic encephalopathies of infancy and childhood (NGS screening panel, 48 genes)

  • Institut für Humangenetik
  • Institut für Humangenetik am Universitätsklinikum Köln
  • Kerpener Str. 34
  • 50931 KÖLN
  • GERMANY
  • Director of laboratory : Pr Brunhilde WIRTH
  • More information
  • Phone : 49 (0)221 478 86464
  • Additional Phone : -
  • Fax : 49 (0)221 478 86465
  • Website
Last update: April 2018

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis
Pre-symptomatic diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
NGS sequencing (except WES)

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.