Universität zu Köln

2014

Hoell, J. I., Gombert, M., Ginzel, S., Loth, S., Landgraf, P., Kaefer, V., Streiter, M., Prokop, A., Weiss, M., Thiele, R. and Borkhardt, A. (2014). Constitutional Mismatch Repair-deficiency and Whole-exome Sequencing as the Means of the Rapid Detection of the Causative MSH6 Defect. Klinische Padiatr., 226 (6-7). S. 357 - 362. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1439-3824