Search Results - "looper, H."

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    PF346 ZEBRAFISH AS A NOVEL MODEL TO STUDY GATA2 HAPLOINSUFFICIENCY SYNDROMES by Gioacchino, E., Koyunlar, C., looper, H., Peulen, J., Bosch, D., hoogenboezem, R., strien, P., Bindels, E., Touw, I., Pater, E.

    Published in HemaSphere (01-06-2019)
    “…Background: Patients with GATA2 mutations have up to 80% chance to develop a myeloid malignancy. MonoMAC and Emberger syndromes are GATA2 deficiency syndromes…”
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    Journal Article
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    S862 THE ROLE OF GATA2 IN HSC GENERATION THROUGH ENDOTHELIAL‐TO‐HEMATOPOIETIC TRANSITION by Koyunlar, C., Gioacchino, E., Hoogenboezem, R., Looper, H., Bosch, D., Klavert, J., Havermans, M., Strien, P., Bindels, E., Delwel, R., Dzierzak, E., Touw, I., Pater, E.

    Published in HemaSphere (01-06-2019)
    “…Background: GATA2 is the most frequently mutated gene in childhood AML. These patients have germline mutations in one allele of GATA2 and have a high…”
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    Journal Article
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