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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

Microarray/Array CGH (Constitutional molecular karyotyping)
2014
NEXTGEN (NextGen DNA Sequencing - pilot scheme)
2014
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.