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Molecular diagnosis of hereditary kidney disease (NGS screening panel: 411 Gene)

  • Institut fr Humangenetik
  • Institut fr Humangenetik am Universittsklinikum Kln
  • Kerpener Str. 34
  • 50931 KLN
  • 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: February 2018

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

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

List of diseases and genes

List of diseases tested (188)
List of genes tested (including panels) (411)
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.