Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | Date | No Grouping
Number of items: 2.

Journal Article

Boztug, Kaan ORCID: 0000-0001-8387-9185, Ding, Xiao-Qi, Hartmann, Hans, Ziesenitz, Lena, Schaeffer, Alejandro A., Diestelhorst, Jana, Pfeifer, Dietmar, Appaswamy, Giridharan, Kehbel, Sonja, Simon, Thorsten, Al Jefri, Abdullah, Lanfermann, Heinrich and Klein, Christoph (2010). HAX1 Mutations Causing Severe Congenital Neuropenia and Neurological Disease Lead to Cerebral Microstructural Abnormalities Documented by Quantitative MRI. Am. J. Med. Genet. A, 152A (12). S. 3157 - 3164. HOBOKEN: WILEY. ISSN 1552-4833

Doering, Jan Henje, Saffari, Afshin, Bast, Thomas, Brockmann, Knut ORCID: 0000-0001-6823-9091, Ehrhardt, Laura, Fazeli, Walid ORCID: 0000-0002-9425-5535, Janzarik, Wibke G., Kluger, Gerhard, Muhle, Hiltrud, Moller, Rikke S., Platzer, Konrad, Santos, Joana Larupa, Bache, Iben ORCID: 0000-0001-7562-8546, Bertsche, Astrid, Bonfert, Michaela, Borggraefe, Ingo, Broser, Philip J., Datta, Alexandre N., Hammer, Trine Bjorg, Hartmann, Hans, Hasse-Wittmer, Anette, Henneke, Marco, Kuehne, Hermann, Lemke, Johannes R., Maier, Oliver, Matzker, Eva, Merkenschlager, Andreas, Opp, Joachim, Patzer, Steffi, Rostasy, Kevin, Stark, Birgit, Strzelczyk, Adam, von Stuelpnagel, Celina, Weber, Yvonne, Wolff, Markus, Zirn, Birgit, Hoffmann, Georg Friedrich, Koelker, Stefan and Syrbe, Steffen (2020). The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood. Biomedicines, 8 (11). BASEL: MDPI. ISSN 2227-9059

This list was generated on Tue Oct 19 01:30:40 2021 CEST.