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- Journal Article
- A1
- open access
European standard clinical practice : key issues for the medical care of individuals with familial leukemia
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- Miscellaneous
- open access
Correction to : functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies
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Association of unbalanced translocation der(1;7) with germline GATA2 mutations
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- Journal Article
- A1
- open access
Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies
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Prevalence, clinical characteristics and prognosis of GATA2-related myelodysplastic syndromes (MDS) in children and adolescents
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Somatic genetic and epigenetic architecture of myelodysplastic syndromes arising from GATA2 deficiency
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Mind the gap : translation of genetic research into clinical care in the context of RUNX1-associated leukaemia predisposition
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Spliceosomal gene aberrations are rare, coexist with oncogenic mutations, and are unlikely to exert a driver effect in childhood MDS and JMML
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Mutations of the spliceosome complex genes occur in adult patients but are very rare in children with myeloid neoplasia
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Therapy-related myelodysplastic syndrome following treatment for childhood acute lymphoblastic leukemia: outcome of patients registered in the EWOG-MDS 98/06 studies