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European Journal of Cancer (Oxford, England : 1990)|December 22, 2021
Circulating tumour DNA sequencing to determine therapeutic response and identify tumour heterogeneity in patients with paediatric solid tumoursReda Stankunaite, Sally L George, Lewis Gallagher, et al.Nature Communications|February 4, 2022
An instructive role for Interleukin-7 receptor α in the development of human B-cell precursor leukemiaIfat Geron, Angela Maria Savino, Hila Fishman, et al.The Journal of Clinical Endocrinology and Metabolism|January 18, 2018
Genetic Analyses in Small-for-Gestational-Age NewbornsSusanne E Stalman, Nita Solanky, Miho Ishida, et al.Nature|October 26, 2022
Phenotypic plasticity and genetic control in colorectal cancer evolutionJacob Househam, Timon Heide, George D Cresswell, et al.American Journal of Human Genetics|December 3, 2014
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndromeAnna C Thomas, Hywel Williams, Núria Setó-Salvia, et al.American Journal of Human Genetics|January 31, 2017
Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia SyndromeMachteld M Oud, Paul Tuijnenburg, Maja Hempel, et al.Pageof 4