Search Results - Lehmann, U.

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    Rare compound heterozygous variants in PNKP identified by whole exome sequencing in a German patient with ataxia-oculomotor apraxia 4 and pilocytic astrocytoma by Scholz, Christian (Author) , Golas, M. M. (Author) , Weber, R. G. (Author) , Hartmann, C. (Author) , Lehmann, U. (Author) , Sahm, Felix (Author) , Schmidt, G. (Author) , Auber, B. (Author) , Sturm, M. (Author) , Schlegelberger, B. (Author) , Illig, T. (Author) , Steinemann, D. (Author) , Hofmann, W. (Author) ,


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    De novo CSF3R mutation associated with transformation of myeloproliferative neoplasm to atypical CML by Bartels, Stefan (Author) , Lehmann, U. (Author) , Büsche, Guntram (Author) , Schlue, Jerome (Author) , Hussein, Kais (Author) , Debatin, Daniel (Author) , Karcher, Andreas (Author) , Andrulis, Mindaugas (Author) , Schirmacher, Peter (Author) , Kreipe, Hans H. (Author) ,


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    Molekularpathologische Diagnostik in der Zytopathologie des nichtkleinzelligen Lungenkarzinoms: Standardisierung der Materialprozessierung by Warth, Arne (Author) , Bubendorf, L. (Author) , Gütz, S. (Author) , Morresi-Hauf, A. (Author) , Hummel, M. (Author) , Junker, K. (Author) , Lehmann, U. (Author) , Petersen, I. (Author) , Schnabel, Philipp Albert (Author) ,


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