Physical map of the Xq27 candidate region for X-linked recessive hypoparathyroidism in two kindreds merged by mitochondrial DNA analysis 由 Mumm, S, Whyte, M, Thakker, R, Schlessinger, D

mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation. 由 Mumm, S, Whyte, M, Thakker, R, Buetow, K, Schlessinger, D

Genome analysis and the human X chromosome. 由 Mandel, J, Monaco, A, Nelson, D, Schlessinger, D, Willard, H

REPORT OF THE 6TH INTERNATIONAL WORKSHOP ON X-CHROMOSOME MAPPING 1995 由 Nelson, D, Ballabio, A, Cremers, F, Monaco, A, Schlessinger, D

REPORT OF THE 5TH INTERNATIONAL WORKSHOP ON HUMAN X-CHROMOSOME MAPPING 1994 由 Willard, H, Cremers, F, Mandel, J, Monaco, A, Nelson, D, Schlessinger, D

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

Expression and cloning of the human X-linked hypophosphatemia gene cDNA. 由 Grieff, M, Mumm, S, Waeltz, P, Mazzarella, R, Whyte, M, Thakker, R, Schlessinger, D

Genetic mapping studies of the X-linked recessive hypoparathyroid gene on the X chromosome (Xq27). 由 Dixon, P, Trump, D, Wooding, C, Mumm, S, Schlessinger, D, Whyte, M, Thakker, R

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

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

Mutations of the PEX regulatory and C-terminal regions cause X-linked hypophosphataemia. 由 Dixon, P, Wooding, C, Christie, P, Grieff, M, Schlessinger, D, Whyte, M, Thakker, R

Characterization of two genes within the candidate region for X-linked spondyloepiphyseal dysplasia tarda. 由 Mumm, S, Huber, R, Waeltz, P, Grieff, M, Thakker, R, Gottesman, G, Whyte, M, Schlessinger, D

Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27. 由 Trump, D, Dixon, P, Mumm, S, Wooding, C, Davies, K, Schlessinger, D, Whyte, M, Thakker, R

Characterization of two genes within the candidate region for X-linked spondyloepiphyseal dysplasia tarda. 由 Mumm, S, Huber, R, Waeltz, P, Grieff, M, Thakker, R, Gottesman, G, Whyte, M, Schlessinger, D

New candidate genes for X-linked recessive hypoparathyroidism. 由 Mumm, S, Zhang, X, Nesbit, M, Mazzarella, R, Schlessinger, D, Thakker, R, Chen, E, Parvari, R, Whyte, M

Genome maps III 由 Mandel, J, Monaco, A, Nelson, D, Schlessinger, D, Willard, H, Chipperfield, M, Pearson, P, Gilna, P, Cinkosky, M

Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22. 由 Miller, A, Gustashaw, K, Wolff, D, Rider, S, Monaco, A, Eble, B, Schlessinger, D, Gorski, J, van Ommen, G, Weissenbach, J

Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1. 由 Trump, D, Pilia, G, Dixon, P, Wooding, C, Thakrar, R, Leigh, SE, Nagaraja, R, Whyte, M, Schlessinger, D, Thakker, R

An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism. 由 Bowl, MR, Nesbit, M, Harding, B, Levy, E, Jefferson, A, Volpi, E, Rizzoti, K, Lovell-Badge, R, Schlessinger, D, Whyte, M, Thakker, R

Mutational analysis of PHEX gene in X-linked hypophosphatemia. 由 Dixon, P, Christie, P, Wooding, C, Trump, D, Grieff, M, Holm, I, Gertner, J, Schmidtke, J, Shah, B, Shaw, N, Smith, C, Tau, C, Schlessinger, D, Whyte, M, Thakker, R