Orphanet: Diagnostik von Mikrodeletions und Mikroduplikations Syndromen durch Mikroarray Analyse
x

Search for a diagnostic test

* (*) mandatory field

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 Klinische Genetik und Tumorgenetik
  • MVZ Institut für Klinische Genetik und Tumorgenetik Bonn GmbH
  • Maximilianstrasse 28D
  • 53111 BONN
  • GERMANY
  • Director of laboratory : Dr Nicolai KOHLSCHMIDT
  • More information
  • Phone : 49 (0)228 96968670
  • Additional Phone : -
  • Fax : 49 (0)228 96968676
  • Website
  • Contact
Last update: April 2013

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
-
-
Cytogenetics
Detection of microdeletions/microduplications
Array based techniques

List of diseases and genes

List of diseases tested (5)
Partial autosomal monosomy
Partial autosomal trisomy/tetrasomy
Partial chromosome Y deletion
Partial deletion of chromosome X
Partial duplication of chromosome X

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.