3-M syndrome: a growth disorder associated with IGF2 silencing

por Murray, P G, Hanson, D, Coulson, T, Stevens, A, Whatmore, A, Poole, R L, Mackay, D J, Black, G C M, Clayton, P E
Publicado 2013

Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics

por Krzyzewska, I. M., Alders, M., Maas, S. M., Bliek, J., Venema, A., Henneman, P., Rezwan, F. I., Lip, K. v. d., Mul, A. N., Mackay, D. J. G., Mannens, M. M. A. M.
Publicado 2019

Epigenotype–phenotype correlations in Silver–Russell syndrome

por Wakeling, E L, Amero, S Abu, Alders, M, Bliek, J, Forsythe, E, Kumar, S, Lim, D H, MacDonald, F, Mackay, D J, Maher, E R, Moore, G E, Poole, R L, Price, S M, Tangeraas, T, Turner, C L S, Van Haelst, M M, Willoughby, C, Temple, I K, Cobben, J M
Publicado 2010

Profound parental bias associated with chromosome 14 acquired uniparental disomy indicates targeting of an imprinted locus

por Chase, A, Leung, W, Tapper, W, Jones, A V, Knoops, L, Rasi, C, Forsberg, L A, Guglielmelli, P, Zoi, K, Hall, V, Chiecchio, L, Eder-Azanza, L, Bryant, C, Lannfelt, L, Docherty, L, White, H E, Score, J, Mackay, D J G, Vannucchi, A M, Dumanski, J P, Cross, N C P
Publicado 2015