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Journal Article

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

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