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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
  • Universitätsklinikum Schleswig-Holstein - Campus Kiel
  • Arnold-Heller-Str. 3
  • 24105 KIEL
  • GERMANY
  • Director of laboratory : Dr Inga VATER
  • More information
  • Phone : 49 (0)431 500 30601
  • Additional Phone : -
  • Fax : 49 (0)431500 30604
  • Website
  • Contact
Last update: April 2013

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

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

Quality management

EQA  EQA

EQA scheme(s) organized by INSTAND

CNV (Array-CGH-analysis)
2015
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.