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Marie Engvall

3PUBLICATIONS
7CO-AUTHORS
Developmental genetics (incl. sex determination)Respiratory diseasesMedical biotechnology diagnostics (incl. biosensors)
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Journal

Publications (3)

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|Apr 06, 2023
Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia.

Anna Eriksson, Marie Engvall, Lucy Mathot

|May 09, 2022
Familial platelet disorder due to germline exonic deletions in <i>RUNX1</i>: a diagnostic challenge with distinct alterations of the transcript isoform equilibrium.

Marie Engvall, Ylva Karlsson, Ekaterina Kuchinskaya

|Jul 31, 2020
Detection of leukemia gene fusions by targeted RNA-sequencing in routine diagnostics.

Marie Engvall, Nicola Cahill, Britt-Inger Jonsson

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Frequent Collaborators

1 joint publications

Anna Eriksson

1 joint publications

Lucy Mathot

1 joint publications

Albin Österroos

1 joint publications

Martin Rippin

1 joint publications

Lucia Cavelier

1 joint publications

Claes Ladenvall

1 joint publications

Panagiotis Baliakas

Frequent Collaborators

1 joint publications

Anna Eriksson

1 joint publications

Lucy Mathot

1 joint publications

Albin Österroos

1 joint publications

Martin Rippin

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