MichaelA Preece

Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome

G. Bell, P. Stanier, D. Monk, 2001, European Journal of Human Genetics.

Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues

P. Stanier, E. Wakeling, G. Moore, 1998, European Journal of Human Genetics.

DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed

G. Kelsey, P. Stanier, D. Monk, 2002, Mammalian Genome.

Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions

P. Stanier, M. Hitchins, G. Moore, 2001, Journal of medical genetics.

Imprinted methylation profiles for proximal mouse Chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis

G. Kelsey, P. Stanier, D. Monk, 2003, Mammalian Genome.

Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.

J. Clayton-Smith, P. Stanier, D. Monk, 2002, Human Genetics.

Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark.

Philip Stanier, Philippe Arnaud, David Monk, 2003, Human molecular genetics.