V. Spencer

Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis.

F. Elmslie, T. Covanis, M. Rees, 1996, Journal of medical genetics.

CAMPATH-1M T-cell depleted BMT for SCID: long-term follow-up of 19 children treated 1987-98 in a single center.

G. Spickett, P. Palmer, A. Dickinson, 2001, Cytotherapy.

Delayed engraftment and mixed chimerism after HLA-identical sibling donor BMT in Fanconi anaemia

R. Skinner, D. Barge, A. Curtis, 1999, Bone Marrow Transplantation.

Co‐dominant Inheritance of Hyperekplexia and Spastic Paraparesis

J. Burn, P. Baxter, S. Connolly, 1996, Developmental medicine and child neurology.