A novel MEN1 intronic mutation associated with multiple endocrine neoplasia type 1. by Lemos, M, Harding, B, Shalet, S, Thakker, R

Compound heterozygous mutations of the AIRE-1 gene causing autoimmune polyendocrinopathy type 1. by Bowl, MR, Turner, J, Nesbit, M, Harding, B, Thakker, R

X-linked hypophosphatemia attributable to pseudoexons of the PHEX gene. by Christie, P, Harding, B, Nesbit, M, Whyte, M, Thakker, R

Cortical neuronal densities and lamination in focal cortical dysplasia. by Thom, M, Martinian, L, Sen, A, Cross, J, Harding, B, Sisodiya, S

Utilisation of a cryptic non-canonical donor splice site of the gene encoding PARAFIBROMIN is associated with familial isolated primary hyperparathyroidism. by Bradley, K, Cavaco, B, Bowl, MR, Harding, B, Young, A, Thakker, R

X-linked hypophosphataemic rickets due to pseudo-exons of the PHEX gene. by Christie, P, Harding, B, Nesbit, M, Eddy, M, Whyte, M, Thakker, R

Proliferation of Pancreatic Islet and Anterior Pituitary Neuroendocrine Tumours (NETs) Developing in a Mouse Model of Multiple Endocrine Neoplasia Type 1 (MEN1) Is Consistent with... by Walls, G, Jeyabalan, J, Reed, A, Hill, N, Harding, B, Thakker, R

Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1. by Bassett, J, Rashbass, P, Harding, B, Forbes, SA, Pannett, A, Thakker, R

Pathological tau tangles localize to focal cortical dysplasia in older patients. by Sen, A, Thom, M, Martinian, L, Harding, B, Cross, J, Nikolic, M, Sisodiya, S

X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase. by Andrew Nesbit, M, Bowl, MR, Harding, B, Schlessinger, D, Whyte, M, Thakker, R

HEREDITARY NEPHROLITHIASIS IS ASSOCIATED WITH MUTATIONS IN AN X-LINKED CHLORIDE CHANNEL GENE by Lloyd, S, Pearce, S, Fisher, S, Harding, B, Scheinman, S, Goodyer, P, Wrong, O, Craig, I, Thakker, R

Proliferation rates of multiple endocrine neoplasia type 1 (MEN1)-associated tumors. by Walls, G, Reed, A, Jeyabalan, J, Javid, M, Hill, N, Harding, B, Thakker, R

Spondyloepimetaphyseal dysplasia, Missouri variant, is located on chromosome 11q22.3 and is caused by a mutation of matrix metalloproteinase 13 (MMP13). by Kennedy, A, Christi, P, Harding, B, Pannett, A, Dearlove, A, Whyte, M, Thakker, R

X-linked recessive hypoparathyroidism is caused by a molecular deletional-insertion involving chromosomes Xq27 and 2p25. by Bowl, MR, Nesbit, M, Harding, B, Levy, E, Schlessinger, D, Whyte, M, Thakker, R

Ataxin-7 aggregation and ubiquitination in infantile SCA7 with 180 CAG repeats. by Ansorge, O, Giunti, P, Michalik, A, Van Broeckhoven, C, Harding, B, Wood, N, Scaravilli, F

A novel EXT1 splice site mutation in a kindred with hereditary multiple exostosis and osteoporosis. by Lemos, M, Kotanko, P, Christie, P, Harding, B, Javor, T, Smith, C, Eastell, R, Thakker, R

Encephalitis lethargica syndrome: 20 new cases and evidence of basal ganglia autoimmunity. by Dale, R, Church, A, Surtees, R, Lees, A, Adcock, J, Harding, B, Neville, BG, Giovannoni, G

CONSTRUCTION AND ANALYSIS OF LINKING LIBRARIES FROM CHROMOSOMES-11 AND XP by Pook, M, Thakrar, R, Harding, B, Porteous, D, Vanheyningen, V, Cowell, J, Jones, C, Davies, K, Thakker, R

UROMODULIN mutations cause familial juvenile hyperuricemic nephropathy. by Turner, J, Stacey, J, Harding, B, Kotanko, P, Lhotta, K, Puig, J, Roberts, I, Torres, R, Thakker, R

Genetic mapping studies of familial juvenile hyperuricemic nephropathy on chromosome 16p11-p13. by Stacey, J, Turner, J, Harding, B, Nesbit, M, Kotanko, P, Lhotta, K, Puig, J, Torres, R, Thakker, R