Search Results - Rabelink, Gwenda

  • Showing 1 - 4 results of 4
Refine Results
  1. 1
    Novel PRKCG/SCA14 mutation in a Dutch spinocerebellar ataxia family: Expanding the phenotype

    Novel PRKCG/SCA14 mutation in a Dutch spinocerebellar ataxia family: Expanding the phenotype by Vlak, Monique H.M., Sinke, Richard J., Rabelink, Gwenda M., Kremer, Berry P.H., van de Warrenburg, Bart P.C.

    Published in Movement disorders
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    Eighteen-year follow-up of a patient with partial hypoxanthine phosphoribosyltransferase deficiency and a new mutation

    Eighteen-year follow-up of a patient with partial hypoxanthine phosphoribosyltransferase deficiency and a new mutation by Gregoric, Alojz, Rabelink, Gwenda M, Kokalj Vokac, Nadja, Varda, Natasa Marcun, Zagradisnik, Boris

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    Cerebellar hypoplasia, zonular cataract, and peripheral neuropathy in trisomy 17 mosaicism

    Cerebellar hypoplasia, zonular cataract, and peripheral neuropathy in trisomy 17 mosaicism by Terhal, Paulien, Sakkers, Ralph, Hochstenbach, Ron, Madan, Kamlesh, Rabelink, Gwenda, Sinke, Richard, Giltay, Jacques

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  4. 4
    Cerebellar hypoplasia, zonular cataract, and peripheral neuropathy in trisomy 17 mosaicism

    Cerebellar hypoplasia, zonular cataract, and peripheral neuropathy in trisomy 17 mosaicism by Terhal, Paulien, Sakkers, Ralph, Hochstenbach, Ron, Madan, Kamlesh, Rabelink, Gwenda, Sinke, Richard, Giltay, Jacques

    Get full text
    Report
    Save to List
    Saved in:

Search Tools: