Orphanet: Diagnostik von Mikrodeletions und Mikroduplikations Syndromen durch Mikroarray Analyse
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Diagnosis of microdeletion and microduplication syndromes by array CGH

Despite our efforts to ensure that data is up to date, this activity has not been validated since 22/04/2013
  • Institut für Humangenetik
  • Biomedizinisches Zentrum
  • Universitätsklinikum Bonn (AöR)
  • Venusberg-Campus 1
  • 53127 BONN
  • GERMANY
  • Director of laboratory : Pr Markus NÖTHEN
  • More information
  • Phone : 49 (0)228 287 51000
  • Additional Phone : 49 (0)228 287 51001
  • Fax : 49 (0)228 287 51011
  • Website
  • Contact
Last update: April 2013

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
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Cytogenetics
Detection of microdeletions/microduplications
Array based techniques

Additional information

Quality management

EQA
 EQA

EQA scheme(s) organized by EMQN

aCGH/ Microarrays
2016, 2017, 2018, 2019
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.