Items where Author is "Schemionek, M."

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Beier, F. and Kirschner, M. and Bouillon, A-S and Halfmeyer, I and Ferreira, Ventura M. and Kricheldorf, K. and Maurer, A. and Wilop, S. and Thol, F. and Roeth, A. and Platzbecker, U. and Radsak, M. and Ayuk, F. A. and Corbacioglu, S. and Hoechsmann, B. and Wilk, C. M. and Hinze, C. and Chromik, J. and Egle, A. and Bittenbring, J. T. and Eggermann, T. and Kurth, I and Koschmieder, S. and Schemionek, M. and Isfort, S. and Panse, J. and Bruemmendorf, T. H. (2018) Identification of patients with classical and/or cryptic dyskeratosis congenita (DKC) by telomere length screening using different percentiles - results from the Aachen telomeropathy registry. KARGER, BASEL.

Kirschner, M. and Bouillon, A. -S. and Ferreira, Ventura M. and Maurer, A. and Wilop, S. and Thol, F. and Roeth, A. and Platzbecker, U. and Blau, W. and Ayuk, F. A. and Corbacioglu, S. and Schrezenmeier, H. and Manz, M. and Ebel, L. and Koschmieder, S. and Schemionek, M. and Isfort, S. and Panse, J. and Brmmendorf, T. H. and Beier, F. (2017) Heterozygous RTEL1 variants are associated with bone marrow failure in cryptic dyskeratosis congenita - first results from the Aachen telomere registry. KARGER, BASEL.