Orphanet: Molecular diagnosis of Acute Myeloid Leukaemia FLT3 itd, NPM1 and cKIT D816V mutation genes and by detection of fusion transcripts: BCRABL and RUNX1RUNX1T1, CBFBMYH11
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Molecular diagnosis of Acute Myeloid Leukaemia (FLT3-itd, NPM1 and cKIT (D816V mutation) genes and by detection of fusion transcripts: BCR/ABL and RUNX1/RUNX1T1, CBFB/MYH11)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 24/11/2011
  • West Midlands Regional Genetics Laboratory (part of the West Midlands Regional Genetics Service)
  • Birmingham Women's NHS Foundation Trust
  • Mindelsohn
  • BIRMINGHAM B15 2TG
  • UNITED KINGDOM
  • Director of laboratory : Dr Mike GRIFFITHS
  • More information
  • Phone : 44 (0)121 627 2710
  • Additional Phone : -
  • Fax : 44 (0)121 627 2711
  • Website
  • Contact
Last update: November 2011

Responsible of diagnostic test

Purpose(s)

Somatic genetics

Technical procedure(s)

Molecular genetics
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List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (9)
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