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Publications by Rudnik-Schöneborn, S.

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Number of items: 2.

Journal article

Braunisch, M. C.; Gallwitz, H.; Abicht, A.; Diebold, I.; Holinski-Feder, E.; Maldergem, L. van; Lammens, M.; Kovacs-Nagy, R.; Alhaddad, B.; Strom, T. M.; Meitinger, T.; Senderek, J.; Rudnik-Schöneborn, S.; Haack, T. B. (2018): Extension of the phenotype of biallelic loss-of-function mutations in SLC25A46 to the severe form of pontocerebellar hypoplasia type I. In: Clinical Genetics, Vol. 93, No. 2: pp. 255-265

Rudnik-Schöneborn, S.; Tölle, D.; Senderek, J.; Eggermann, K.; Elbracht, M.; Kornak, U.; Hagen, M. von der; Kirschner, J.; Leube, B.; Müller-Felberg, W.; Scharah, U.; Au, K. von; Wieczorek, D.; Bußmann, C.; Zerres, K. (2016): Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patients. In: Clinical Genetics, Vol. 89, No. 1: pp. 34-43

This list was generated on Sun Dec 15 08:20:08 2019 CET.