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Author

D. Fedorova

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Review Open access Aug 2026

Rare inherited bone marrow failure syndromes with cancer predisposition associated with SRP72, SH2B3, MYSM1 and CBL variants: a literature review and case series

The findings highlight the importance of early molecular genetic testing in children with persistent hematopoietic abnormalities, along with regular cytogenetic surveillance and timely referral of high-risk patients for HSCT.

M. S. Vasilyeva, A. Pavlova, D. Fedorova et al. · 0 citations

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