Robin Andersson

Robin Andersson

Lektor


  1. 2007
  2. A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene

    Mikhail, F. M., Descartes, M., Piotrowski, A., Andersson, Robin, Diaz de Ståhl, T., Komorowski, J., Bruder, C. E. G., Dumanski, J. P. & Carroll, A. J., 15 sep. 2007, I: American Journal of Medical Genetics. Part A. 143A, 18, s. 2178-84 7 s.

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  3. Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter)

    Mikhail, F. M., Sathienkijkanchai, A., Robin, N. H., Prucka, S., Biggerstaff, J. S., Komorowski, J., Andersson, Robin, Bruder, C. E. G., Piotrowski, A., Diaz de Ståhl, T., Dumanski, J. P. & Carroll, A. J., 1 aug. 2007, I: American Journal of Medical Genetics. Part A. 143A, 15, s. 1760-6 7 s.

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  4. 2005
  5. RoSy: A Rough Knowledge Base System

    Andersson, Robin, Vitória, A., Małuszyński, J. & Komorowski, J., 2005, Rough Sets, Fuzzy Sets, Data Mining, and Granular Computing. Slezak, D., Yao, J., Peters, J. F., Ziarko, W. & Hu, X. (red.). Springer, s. 48-58 11 s. (Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics), Bind 3642 LNAI).

    Publikation: Bidrag til bog/antologi/rapportKonferencebidrag i proceedingsForskningfagfællebedømt

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