Walne, A. J., Vulliamy, T., Beswick, R., Kirwan, M., & Dokal, I. (2010). Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund–Thomson syndrome. Oxford University Press.

Walne, Amanda J., Tom Vulliamy, Richard Beswick, Michael Kirwan, i Inderjeet Dokal. Mutations in C16orf57 and Normal-length Telomeres Unify a Subset of Patients With Dyskeratosis Congenita, Poikiloderma With Neutropenia and Rothmund–Thomson Syndrome. Oxford University Press, 2010.

Walne, Amanda J., et al. Mutations in C16orf57 and Normal-length Telomeres Unify a Subset of Patients With Dyskeratosis Congenita, Poikiloderma With Neutropenia and Rothmund–Thomson Syndrome. Oxford University Press, 2010.