BIRTH DEFECTS RES - Birth Defects Research

Publications

  1. 2017
  2. Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations

    Zhang, R., Marsch, F., Kause, F., Degenhardt, F., Schmiedeke, E., Märzheuser, S., Hoppe, B., Bachour, H., Boemers, T. M., Schäfer, M., Spychalski, N., Neser, J., Leonhardt, J., Kosch, F., Ure, B., Gómez, B., Lacher, M., Deffaa, O. J., Palta, M., Wittekindt, B., Kleine, K., Schmedding, A., Grasshoff-Derr, S., Ven, A. V. D., Heilmann-Heimbach, S., Zwink, N., Jenetzky, E., Ludwig, M. & Reutter, H., 17.07.2017, In: BIRTH DEFECTS RES. 109, 13, p. 1063-1069 7 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review