Browse by Person

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 6.


Hepburn, L., Prajsnar, T.K., Klapholz, C. et al. (29 more authors) (2014) A Spaetzle-like role for nerve growth factor beta in vertebrate immunity to Staphylococcus aureus. SCIENCE, 346 (6209). pp. 641-646. ISSN 0036-8075

Lynex, C.N., Carr, I.M., Leek, J.P. et al. (6 more authors) (2004) Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndrome and other movement disorders. BMC Neurology, 4 (20). ISSN 1471-2377

Mubaidin, A., Roberts, E., Hampshire, D. et al. (7 more authors) (2003) Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum. Journal of Medical Genetics, 40 (7). pp. 543-546. ISSN 0022-2593

Leal, G.F., Roberts, E., Silva, E.O. et al. (3 more authors) (2003) A novel locus for autosomal recessive primary microcephaly (MCPH6) maps to 13q12.2. Journal of Medical Genetics, 40 (7). pp. 540-542. ISSN 0022-2593

Roberts, E., Hampshire, D.J., Pattison, L. et al. (8 more authors) (2002) Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation. Journal of Medical Genetics, 39 (10). pp. 718-721. ISSN 0022-2593

Hampshire, D.J., Roberts, E., Crow, Y. et al. (5 more authors) (2001) Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36. Journal of Medical Genetics, 38 (10). pp. 680-682. ISSN 0022-2593

This list was generated on Sat Jan 18 22:28:10 2020 GMT.