Showing 1 - 8 results of 8 for search 'Grieff, M', query time: 0.02s
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Sequence analysis of 139 kb in Xp22.1 containing spermine synthase and the 5' region of PEX. by Grieff, M, Whyte, M, Thakker, R, Mazzarella, R
Published 1997Journal article -
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Expression and cloning of the human X-linked hypophosphatemia gene cDNA. by Grieff, M, Mumm, S, Waeltz, P, Mazzarella, R, Whyte, M, Thakker, R, Schlessinger, D
Published 1997Journal article -
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Mutations of the PEX regulatory and C-terminal regions cause X-linked hypophosphataemia. by Dixon, P, Wooding, C, Christie, P, Grieff, M, Schlessinger, D, Whyte, M, Thakker, R
Published 1997Journal article -
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Characterization of two genes within the candidate region for X-linked spondyloepiphyseal dysplasia tarda. by Mumm, S, Huber, R, Waeltz, P, Grieff, M, Thakker, R, Gottesman, G, Whyte, M, Schlessinger, D
Published 1997Journal article -
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Characterization of two genes within the candidate region for X-linked spondyloepiphyseal dysplasia tarda. by Mumm, S, Huber, R, Waeltz, P, Grieff, M, Thakker, R, Gottesman, G, Whyte, M, Schlessinger, D
Published 1997Journal article -
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X-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotype by Whyte, M, Christie, P, Podgornik, M, Dixon, P, Eddy, M, Wooding, C, Trump, D, Grieff, M, Mumm, S, Shlessinger, D, Thakker, R
Published 1999Journal article -
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Mutational analysis of PHEX gene in X-linked hypophosphatemia. by 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
Published 1998Journal article