 | Up a level |
2019
Renner, Sina, Schueler, Helke, Alawi, Malik, Kolbe, Verena, Rybczynski, Meike, Woitschach, Rixa, Sheikhzadeh, Sara, Stark, Veronika C., Olfe, Jakob, Roser, Elke, Seggewies, Friederike Sophia, Mahlmann, Adrian, Hempel, Maja, Hartmann, Melanie J., Hillebrand, Mathias, Wieczorek, Dagmar, Volk, Alexander Erich, Kloth, Katja, Koch-Hogrebe, Margarete, Abou Jamra, Rami, Mitter, Diana, Altmueller, Janine, Wey-Fabrizius, Alexandra, Petersen, Christine, Rau, Isabella, Borck, Guntram, Kubisch, Christian, Mir, Thomas S., von Kodolitsch, Yskert, Kutsche, Kerstin and Rosenberger, Georg (2019). Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients. Genet. Med., 21 (8). S. 1832 - 1842. NEW YORK: NATURE PUBLISHING GROUP. ISSN 1530-0366
2016
Dunkl, Veronika, Rau, Isabella, Wunderlich, Gilbert, Fink, Gereon R. 
ORCID: 0000-0002-8230-1856 and Lehmann, Helmar C.
(2016).
Oligosymptomatic adrenomyeloneuropathy due to a novel mutation in the ABCD1 start codon.
J. Neurol. Sci., 367.
S. 81 - 83.
AMSTERDAM:
ELSEVIER SCIENCE BV.
ISSN 1878-5883