Ben Curran

发表

Complex Patterns of Genomic Heterogeneity Identified in 42 Tumor Samples and ctDNA of a Pulmonary Atypical Carcinoid Patient

C. Print, C. Blenkiron, P. Tsai, 2022, Cancer research communications.

Biallelic ATP2B1 variants as a likely cause of a novel neurodevelopmental malformation syndrome with primary hypoparathyroidism

P. Kakadia, L. Riley, Meer Jacob Rahimi, 2023, European journal of human genetics : EJHG.