BIRTH DEFECTS RES - Birth Defects Research
Publications
- 2017
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 journal › SCORING: Journal article › Research › peer-review