Orphanet: Diagnostique mol�culaire de syndrome et de pr�disposition � la leuc�mie my�lo�de aigu�
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Molecular diagnosis of Acute Myeloid Leukaemia (FLT3, NPM, CEBPA, PML-RARa, CBFB-MYH11, RUNX1-RUNX1T1, mutation D816V of c-KIT)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 23/06/2015
  • Laboratoire de gntique molculaire hmato-oncologique
  • Service de Gntique Mdicale
  • Erasme Hospital - ULB
  • Route de Lennik 808
  • 1070 BRUSSELS
  • BELGIUM
  • Director of laboratory : Pr Guillaume SMITS
  • More information
  • Phone : 0032 2 5554145
  • Additional Phone : -
  • Fax : 0032 2 5554212
  • Website
Last update: June 2015

Responsible of diagnostic test

Purpose(s)

Somatic genetics

Technical procedure(s)

Molecular genetics
Mutation scanning/screening and sequence analysis of selected exons
Sanger sequencing

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (4)

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.