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  • Wieacker, P
Showing 1 - 2 results of 2 for search 'Wieacker, P', query time: 0.02s Refine Results
  1. 1
    Greig Cephalopolysyndactyly (GCPS) Contiguous Gene Syndrome in a Boy with a 14 Mb Deletion in Region 7p13-14 Caused by a Paternal Balanced Insertion (5; 7) [Expression of Concern]

    Greig Cephalopolysyndactyly (GCPS) Contiguous Gene Syndrome in a Boy with a 14 Mb Deletion in Region 7p13-14 Caused by a Paternal Balanced Insertion (5; 7) [Expression of Concern] by Schulz S, Volleth M, Muschke P, Wieland I, Wieacker P

    Published 2021-03-01
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    Article
  2. 2
    Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin.

    Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin. by Hennies, H, Kornak, U, Zhang, H, Egerer, J, Zhang, X, Seifert, W, Kühnisch, J, Budde, B, Nätebus, M, Brancati, F, Wilcox, W, Müller, D, Kaplan, P, Rajab, A, Zampino, G, Fodale, V, Dallapiccola, B, Newman, W, Metcalfe, K, Clayton-Smith, J, Tassabehji, M, Steinmann, B, Barr, F, Nürnberg, P, Wieacker, P

    Published 2008
    Journal article

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