Linda S. Weaving

MECP2 and Beyond: Phenotype—Genotype Correlations in Rett Syndrome

J. Christodoulou, L. Weaving, Linda S. Weaving, 2003, Journal of child neurology.

Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation.

J. Gécz, A. Clarke, P. Tam, 2004, American journal of human genetics.

Epigenetic effects on transgene expression.

E. Whitelaw, D. Garrick, H. Morgan, 2001, Methods in molecular biology.

Rett syndrome: clinical review and genetic update

J. Gécz, J. Christodoulou, C. Ellaway, 2005, Journal of Medical Genetics.

Health Service Use in Rett Syndrome

J. Christodoulou, H. Leonard, N. de Klerk, 2005, Journal of child neurology.

Trisomy 21 and Rett syndrome: A double burden

J. Christodoulou, H. Leonard, M. Delatycki, 2004, Journal of paediatrics and child health.