E. Thompson

Lost in translation: translational interference from a recurrent mutation in exon 1 of MECP2

J. Christodoulou, H. Leonard, D. Ravine, 2005, Journal of Medical Genetics.

Mutation analysis in the MECP2 gene and genetic counselling for Rett syndrome

F. Hanefeld, A. Clarke, J. Christodoulou, 2003, Journal of medical genetics.

The need to screen all retinoblastoma patients for esterase D activity: detection of submicroscopic chromosome deletions.

J. Cowell, P. Rutland, E. Thompson, 1987, Archives of disease in childhood.

deletions . submicroscopic chromosome esterase D activity : detection of retinoblastoma patients for The need to screen all

J. Cowell, P. Rutland, E. Thompson, 2022 .

Reduced penetrance alleles for Huntington’s disease: a multi-centre direct observational study

A. Rigby, F. Raymond, M. Losekoot, 2006, Journal of Medical Genetics.

Exclusion mapping of polycystic kidney disease: A third locus

E. Thompson, 1998 .