Zeynep Tümer

Zeynep Tümer

Clinical Professor

Member of:

  • Clinical Genetics


Publication year:
All
1 - 4 out of 4Page size: 10
  1. 2010
  2. Published

    Deletion of 7q34-q36.2 in two siblings with mental retardation, language delay, primary amenorrhea, and dysmorphic features

    Sehested, L. T., Møller, R. S., Bache, Iben, Andersen, N. B., Ullmann, R., Tommerup, Niels & Tümer, Asuman Zeynep, 1 Dec 2010, In: American Journal of Medical Genetics. Part A. 152A, 12, p. 3115-9 5 p.

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

  3. Published

    Haploinsufficiency of TAB2 causes congenital heart defects in humans

    Thienpont, B., Zhang, L., Postma, A. V., Breckpot, J., Tranchevent, L., Van Loo, P., Møllgård, Kjeld, Tommerup, Niels, Bache, Iben, Tümer, Asuman Zeynep, van Engelen, K., Menten, B., Mortier, G., Waggoner, D., Gewillig, M., Moreau, Y., Devriendt, K. & Larsen, Lars Allan, 2010, In: American Journal of Human Genetics. 86, 6, p. 839-49 10 p.

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

  4. Published

    Menkes disease

    Tümer, Asuman Zeynep & Møller, L. B., 2010, In: European Journal of Human Genetics. 18, 5, p. 511-8 7 p.

    Research output: Contribution to journal › Review › Research

  5. Published

    Molecular genetic mutation analysis in Menkes-disease with prenatal diagnosis

    László, A., Endreffy, E., Tümer, Asuman Zeynep, Horn, N. & Szabó, J., 2010, In: Ideggyógyászati szemle. 63, 1-2, p. 48-51 3 p.

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

ID: 7071