Orphanet: Diagnostik akuter myeloischer Leuk�mien Fusionsgene und Rearrangements: RUNX1 RUNX1T1 AML1 ETO, CBFB MYH11, PML RARA, MLLT3 MLL AF9 MLL, DEK NUP214 DEK CAN, RPN1 EVI1, RBM15 MKL1, MLL, RUNX1 EVI1 Aberrationen von Chromosom 17 17p13 TP53, 55q, 77q Mutationsanalyse von FLT TKD, WT1, C KIT, N RAS, GATA1, GATA2, RUNX1 AML1, CEBPA
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Diagnosis of acute myeloblastic leukemia (fusion genes and rearrangements: RUNX1-RUNX1T1 (AML1-ETO), CBFB-MYH11, PML-RARA, MLLT3-MLL (AF9-MLL), DEK-NUP214 (DEK-CAN), RPN1-EVI1, RBM15-MKL1, MLL, RUNX1-EVI1; aberrations of chromosom 17 (17p13 / TP53), 5/5q, 7/7q; mutation analysis of FLT-TKD, WT1, C- KIT, N- RAS, GATA1, GATA2, RUNX1 (AML1), CEBPA)

  • Institut fr Humangenetik
  • Zentrum Pathologie, Forensik und Genetik
  • Medizinische Hochschule Hannover
  • Carl-Neuberg-Str. 1
  • 30625 HANNOVER
  • GERMANY
  • Director of laboratory : Pr Brigitte SCHLEGELBERGER
  • More information
  • Phone : 49 (0)511 532 4520
  • Additional Phone : -
  • Fax : 49 (0)511 532 4521
  • Website
  • Contact
Last update: June 2017

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis
Somatic genetics

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
PCR based techniques
Sequence analysis: entire coding region
Sanger sequencing
Cytogenetics
Detection of microdeletions/microduplications
FISH
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.