LOCALIZATION OF THE GENE CAUSING X-LINKED RECESSIVE NEPHROLITHIASIS TO THE SHORT ARM OF THE X-CHROMOSOME (XP11.22) by Scheinman, S, Wooding, C, Frymoyer, P, Thakker, R

X-linked hypophosphataemic rickets in a Saudi Arabian kindred results from a nonsense mutation of the PEX gene. by Dixon, P, Wooding, C, Cristie, P, Thakker, R

MOLECULAR GENETIC-ANALYSIS OF THE MOUSE X-LINKED HYPOPHOSPHATEMIA LOCUS BY USE OF AN INTERSPECIFIC BACKCROSS AND LINKING CLONES by Thakker, R, Brockdorff, N, Kay, G, Wooding, C, Rastan, S

MOLECULAR-GENETIC ANALYSIS OF THE MOUSE X-LINKED HYPOPHOSPHATEMIA LOCUS BY USE OF AN INTERSPECIFIC BACKCROSS AND LINKING CLONES by Thakker, R, Brockdorff, N, Kay, G, Wooding, C, Rastan, S

MAPPING OF THE X-LINKED IDIOPATHIC HYPOPARATHYROID GENE TO XQ26-XQ27 BY LINKAGE STUDIES by Thakker, R, Davies, K, Whyte, M, Wooding, C, Oriordan, J

CHROMOSOME-11 ABNORMALITIES IN SOMATOTROPHINOMAS FROM PATIENTS WITH ACROMEGALY by Thakker, R, Wooding, C, Boscaro, M, Scanarini, M, Clayton, R

Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22. by Pook, M, Wrong, O, Wooding, C, Norden, A, Feest, T, Thakker, R

Loss of heterozygosity studies at the retinoblastoma and breast cancer susceptibility (BRCA2) loci in pituitary, parathyroid, pancreatic and carcinoid tumours. by Pearce, S, Trump, D, Wooding, C, Sheppard, M, Clayton, R, Thakker, R

Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies. by Scheinman, S, Pook, M, Wooding, C, Pang, J, Frymoyer, P, Thakker, R

THE GENE CAUSING DENTS DISEASE, A RENAL FANCONI SYNDROME WITH NEPHROCALCINOSIS AND KIDNEY-STONES, IS ON THE SHORT ARM OF THE X-CHROMOSOME (XP11.22) by Thakker, R, Pook, M, Wooding, C, Norden, A, Feest, T, Wrong, O

Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies. by Thakker, R, Davies, K, Whyte, M, Wooding, C, O'Riordan, J

Calcium-sensing receptor mutations in familial hypocalciuric hypercalcaemia with recurrent pancreatitis. by Pearce, S, Wooding, C, Davies, M, Tollefsen, SE, Whyte, M, Thakker, R

MAPPING OF 2 HEREDITARY RENAL TUBULAR DISORDERS ASSOCIATED WITH KIDNEY-STONES, AND REFERRED TO AS DENT-DISEASE AND X-LINKED RECESSIVE NEPHROLITHIASIS, TO CHROMOSOME-XP11 by Thakker, R, Pang, J, Wooding, C, Scheinman, S, Wrong, O, Pook, M

Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations. by Thakker, R, Pook, M, Wooding, C, Boscaro, M, Scanarini, M, Clayton, R

LINKAGE STUDIES IN A KINDRED WITH HYPOCALCIURIC HYPERCALCEMIA AND INCREASING SERUM PARATHYROID-HORMONE LEVELS INDICATE GENETIC-HETEROGENEITY by Trump, D, Whyte, M, Wooding, C, Pang, J, Kocher, D, Thakker, R

LINKAGE STUDIES IN A KINDRED FROM OKLAHOMA WITH FAMILIAL BENIGN HYPOCALCIURIC HYPERCALCEMIA (FBH) INDICATE GENETIC-HETEROGENEITY AND A 3RD LOCUS FOR FBH by Trump, D, Whyte, M, Wooding, C, Pang, J, Kocher, D, Thakker, R

Seven novel mutations in the PEX gene indicate molecular heterogeneity for X-linked hypophosphataemic rickets. by Dixon, P, Wooding, C, Trump, D, Schlessinger, D, Whyte, M, Thakker, R

LINKAGE ANALYSIS OF 3 CLONED DNA-SEQUENCES, DXS294, CDR AND DXS105, IN X-LINKED RECESSIVE HYPOPARATHYROID FAMILIES by Thakker, R, Wooding, C, Parkinson, D, Blake, D, Whyte, M, Davies, K

MOLECULAR-GENETIC MAPPING OF 13 MARKERS FROM CHROMOSOME-11Q13 IN 33 FAMILIES WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 by Pang, J, Wooding, C, Leigh, S, Taggart, R, Sheffield, V, Jones, C, Thakker, R

Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a t... by Trump, D, Whyte, M, Wooding, C, Pang, J, Pearce, S, Kocher, D, Thakker, R