Orphanet: Diagnostic de la leuc�mie aigu� lymphoblastique d�tection des fusions CBFB MYH11, PML RARA, RUNX1 RUNX1T1 et s�quen�age des g�nes NPM1 et FLT3
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'Diagnosis of acute lymphoblastic leukemia (detection of CBFB-MYH11, PML-RARA, RUNX1-RUNX1T1 fusion genes; FLT3 and NPM1 gene sequencing)'

  • Laboratoire d'Hmatologie - Secteur de cytogntique et biologie molculaire
  • CHU de Bordeaux-GH Sud - Hpital Haut-Lvque
  • 1 avenue Magellan
  • 33604 PESSAC CEDEX
  • FRANCE
  • Director of laboratory : Dr Audrey BIDET
  • More information
  • Phone : 33 (0)5 57 65 64 78
  • Additional Phone : -
  • Fax : 33 (0)5 57 65 68 45
  • Website
  • Contact
Last update: August 2018

Responsible of diagnostic test

Purpose(s)

Somatic genetics

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
PCR based techniques
Sequence analysis: entire coding region
Sanger sequencing

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (8)
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.