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1. Biallelic variants in BRCA1 gene cause a recognisable phenotype within chromosomal instability syndromes reframed as BRCA1 deficiency. Issue 9 (25th August 2020)

4. OC-65 Hemophagocytic lymphohistiocytosis – the importance of an earlier diagnosis and treatment in paediatric practice. (6th June 2017)