Munich Leukemia Laboratory Leukemia diagnostics for safe lab results with diagnostics laboratory MLL


We are the interdisciplinary experts

Our optimized diagnoses based on an extensive spectrum of methods help to extend life expectancy with improved quality of life.

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The foundation for a specific therapy

Expertise, focus topics, state-of-the-art technology and tireless research – combined with our unwavering commitment to progress – guarantee optimized and individual diagnosis.

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New: Englisch lab request form

Please see our new English lab request form including a detailed overview of the spectrum of our hematological diagnostics.

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    Samples received since 2005

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MLL Magazine

Stay up to date

Here you will find all MLL News as well as scientific contributions to leukemia diagnostics and research.

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Current Articles

  • Dr. rer. nat. Frank Dicker
    from 14.06.2021
    4-stage (4-tier) system for evaluating sequence variants

    Sequence alterations have classically been divided into two categories: "mutation" and "polymorphism". However, the rapid increase in sequencing data from healthy and various diseased tissues has made it obvious that there is a broad spectrum between clearly disease-associated pathogenic alterations and non-pathogenic polymorphisms. As of now, we are working in molecular genetics with the world's most widely used 4-tier classification system, which we have adapted to central questions in hematological diagnostics. We would like to introduce this to you in this article.

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  • Prof. Dr. med. Dr. phil. Torsten Haferlach
    from 11.06.2021
    The logic of next generation sequencing wherever myeloid neoplasia is suspected

    Recently, S. Vantyghem et al (Haematologica 3/1/2021, pages 701–707) published a “real-life study.” The analyses were focused on 177 patients with suspected or already confirmed myeloid neoplasias such as MDS or MPN without a final diagnosis using cytomorphology and immunophenotyping. In a first cohort, an NGS panel with 34 genes was used either to exclude or confirm a definitive diagnosis. In a second cohort, the extent to which prognostic and especially therapeutic consequences would have to be drawn if somatic mutations were detectable was investigated. I would like to introduce this study to you in this article.

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