ing. M. Benjamins-Stok

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E-mail:
m.benjamins umcg.nl

Research

Publications
  1. Segmental and total uniparental isodisomy (UPiD) as a disease mechanism in autosomal recessive lysosomal disorders: evidence from SNP arrays

    Labrijn-Marks, I., Somers-Bolman, G. M., Groen, S. L. M. I., Hoogeveen-Westerveld, M., Kroos, M. A., Ala-Mello, S., Amaral, O., Miranda, C. S., Mavridou, I., Michelakakis, H., Naess, K., Verheijen, F. W., Hoefsloot, L. H., Dijkhuizen, T., Benjamins, M., van den Hout, H. J. M., van der Ploeg, A. T., Pijnappel, W. W. M. P., Saris, J. J. & Halley, D. J., Jun-2019, In : European Journal of Human Genetics. 27, 6, p. 919-927 9 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  2. Toward an effective exome-based genetic testing strategy in pediatric dilated cardiomyopathy

    Herkert, J. C., Abbott, K. M., Birnie, E., Meems-Veldhuis, M. T., Boven, L. G., Benjamins, M., Sarvaas, G. J. D. M., Barge-Schaapveld, D. Q. C. M., van Tintelen, J. P., van der Zwaag, P. A., Vos, Y. J., Sinke, R. J., van den Berg, M. P., van Langen, I. M. & Jongbloed, J. D. H., Nov-2018, In : Genetics in Medicine. 20, 11, p. 1374-1386 13 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  3. Identification of prognostic relevant chromosomal abnormalities in chronic lymphocytic leukemia using microarray-based genomic profiling

    Stevens-Kroef, M. J. P. L., van den Berg-de Ruiter, E., Weghuis, D. O., van Kessel, A. G., Pfundt, R., Linssen-Wiersma, M., Benjamins, M., Dijkhuizen, T., Groenen, P. J. T. A. & Simons, A., 9-Jan-2014, In : Molecular Cytogenetics. 7, 11 p., 3.

    Research output: Contribution to journalArticleAcademicpeer-review

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