Authors:
Watson, P
Black, G
Ramsden, S
Barrow, M
Super, M
Kerr, B
Clayton-Smith, J
Citation: P. Watson et al., Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein, J MED GENET, 38(4), 2001, pp. 224-228
Authors:
Lako, M
Ramsden, S
Campbell, RD
Strachan, T
Citation: M. Lako et al., Mutation screening in British 21-hydroxylase deficiency families and development of novel microsatellite based approaches to prenatal diagnosis, J MED GENET, 36(2), 1999, pp. 119-124
Citation: S. Ramsden, The child and adolescent psychotherapist in a hospital setting, HANDBOOK OF CHILD AND ADOLESCENT PSYCHOTHERAPY, 1999, pp. 141-158