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Diagnosis of hemoglobinopathies (HBA1, HBA2, HBB genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 07/03/2017
  • Institut fr Klinische Genetik
  • Klinikum Stuttgart - Standort Olgahospital
  • Kriegsbergstrae 62
  • 70174 STUTTGART
  • GERMANY
  • Director of laboratory : Dr Martina WLFLE
  • More information
  • Phone : 49 (0)711 278 74 001
  • Additional Phone : -
  • Fax : 49 (0)711 278 74 000
  • Website
Last update: March 2017

Responsible of diagnostic test

Purpose(s)

Antenatal diagnosis
Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing
Deletion / Duplication analysis
MLPA based techniques

Additional information

Quality management

EQA
 EQA

EQA scheme(s) organized by INSTAND

Molekulargenetik SET 20: alpha-globin, beta-globin
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.