Showing 1 - 2 results of 2 for search 'G. Matthijs', query time: 0.03s Refine Results
  1. 1
    A PMM2-CDG caused by an A108V mutation associated with a heterozygous 70 kilobases deletion case report

    A PMM2-CDG caused by an A108V mutation associated with a heterozygous 70 kilobases deletion case report by E. Lebredonchel, A. Riquet, D. Neut, F. Broly, G. Matthijs, A. Klein, F. Foulquier

    Published 2022-10-01
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    Article
  2. 2
    ALG11-CDG: Three novel mutations and further characterization of the phenotype

    ALG11-CDG: Three novel mutations and further characterization of the phenotype by L. Regal, P.M. van Hasselt, F. Foulquier, I. Cuppen, HCMT Prinsen, K. Jansen, L. Keldermans, L. De Meirleir, G. Matthijs, J. Jaeken

    Published 2015-03-01
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    Article

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