Robin Andersson

Robin Andersson

Associate Professor

ORCID: 0000-0003-1516-879X

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  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, In: American Journal of Medical Genetics. Part A. 143A, 18, p. 2178-84 7 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  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, In: American Journal of Medical Genetics. Part A. 143A, 15, p. 1760-6 7 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

ID: 32384007