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

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

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

REPORT OF THE 5TH INTERNATIONAL WORKSHOP ON HUMAN X-CHROMOSOME MAPPING 1994 Tekijä 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. Tekijä Dixon, P, Wooding, C, Trump, D, Schlessinger, D, Whyte, M, Thakker, R

Expression and cloning of the human X-linked hypophosphatemia gene cDNA. Tekijä 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). Tekijä 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. Tekijä 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. Tekijä 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. Tekijä 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. Tekijä 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. Tekijä 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. Tekijä Mumm, S, Huber, R, Waeltz, P, Grieff, M, Thakker, R, Gottesman, G, Whyte, M, Schlessinger, D

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

Genome maps III Tekijä 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. Tekijä 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. Tekijä 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. Tekijä 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. Tekijä 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