Autor/in Kutsche, K Bierhals, T 2 Kortüm, F 2 Abdollahpour, H 1 Alawi, M 1 Altmüller, J 1 Bartels, I 1 Bayer, J 1 Bergmann, C 1 Burfeind, P 1 Chilian, B 1 Fekete, G 1 Frank, V 1 Freitag, S 1 Haltrich, I 1 Harms, F L 1 Kneussel, M 1 Kodolitsch, Yskert 1 Liehr, T 1 Muhia, M 1 Nagel, I 1 Nampoothiri, S 1 Panicker, V V 1 Rosenberger, G 1 Rune, G M 1 Schmidt, T 1 Shoukier, M 1 Sommer-Blöchl, Tobias 1 Thomas, J 1 Vierk, R 1 Wolbers, T 1 Yesodharan, D 1 alle zeigenListe einklappen
Coinheritance of biallelic SLURP1 and SLC39A4 mutations cause a severe genodermatosis with skin peeling and hair loss all over the body Harms, F L Nampoothiri, S Kortüm, F Thomas, J Panicker, V V Alawi, M Altmüller, J 2018 - Forschungsinformationssystem des UKE
Genetic diagnostics of inherited aortic diseases: Medical strategy analysis Kodolitsch, Yskert Kutsche, K 2017 - Forschungsinformationssystem des UKE
Structure-function-behavior relationship in estrogen-induced synaptic plasticity Vierk, R Bayer, J Freitag, S Muhia, M Kutsche, K Wolbers, T Kneussel, M 2015 - Forschungsinformationssystem des UKE
Branchio-otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8 Schmidt, T Bierhals, T Kortüm, F Bartels, I Liehr, T Burfeind, P Shoukier, M 2014 - Forschungsinformationssystem des UKE
Dysfunction of SHANK2 and CHRNA7 in a patient with intellectual disability and language impairment supports genetic epistasis of the two loci Chilian, B Abdollahpour, H Bierhals, T Haltrich, I Fekete, G Nagel, I Rosenberger, G 2013 - Forschungsinformationssystem des UKE