Associated Papers
Distinctive phenotypes in two children with novel germline RUNX1 mutations - one with myeloid malignancy and increased fetal hemoglobin.
Bagla S et al.
Pediatric Hematology and Oncology, 2021
Mutational landscape and genetic signatures of cell-free DNA in tumour-induced osteomalacia.
Wu N et al.
Journal of Cellular and Molecular Medicine, 2020
32277576 (PubMed )
Supplement: JCMM-24-4931-s011.xlsx › Sheet1
Inactivating CUX1 mutations promote tumorigenesis.
Wong CC et al.
Nature Genetics, 2014
24316979 (PubMed )
Supplement: NIHMS55610-supplement-2.xlsx › Sup_table_3
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