Showing 1 - 3 results of 3 for search 'Weiss Marjan M', query time: 0.01s Refine Results
  1. 1
    Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma

    Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma by Wong Nora, Ferrando Barbara, Pasini Barbara, Menko Fred H, Oomen Peter HN, Jansen Jeroen C, Weiss Marjan M, van Minderhout Ivonne, Bayley Jean-Pierre, Alpert Lesley C, Williams Rosie, Blair Edward, Devilee Peter, Taschner Peter EM

    Published 2006
    Connect to this object online.
    Book
    Save to List
    Saved in:
  2. 2
    The first Dutch <it>SDHB </it>founder deletion in paraganglioma - pheochromocytoma patients

    The first Dutch <it>SDHB </it>founder deletion in paraganglioma - pheochromocytoma patients by Devilee Peter, Dullaart Robin PF, Jansen Jeroen C, Lenders Jacques W, Kunst Henricus P, van der Wielen Michiel, van Bunderen Patrick A, Grimbergen Anneliese EM, Bayley Jean-Pierre, Corssmit Eleonora P, Vriends Annette H, Losekoot Monique, Weiss Marjan M

    Published 2009
    Connect to this object online.
    Book
    Save to List
    Saved in:
  3. 3
    Low penetrance of a <it>SDHB </it>mutation in a large Dutch paraganglioma family

    Low penetrance of a <it>SDHB </it>mutation in a large Dutch paraganglioma family by Jansen Jeroen C, Romijn Johannes A, Morreau Hans, Stokkel Marcel PM, Bonsing Bert A, van Bunderen Patrick A, de Miranda Noel F, Woortman Sanne A, Weiss Marjan M, Hes Frederik J, Vriends Annette HJT, Bayley Jean-Pierre L, Corssmit Eleonora PM

    Published 2010
    Connect to this object online.
    Book
    Save to List
    Saved in:

Search Tools: