5 Einträge gefunden

1. Coinheritance of biallelic SLURP1 and SLC39A4 mutations cause a severe genodermatosis with skin peeling and hair loss all over the body

   1. Harms, F L
   2. Nampoothiri, S
   3. Kortüm, F
   4. Thomas, J
   5. Panicker, V V
   6. Alawi, M
   7. Altmüller, J

   2018 - Forschungsinformationssystem des UKE
2. Genetic diagnostics of inherited aortic diseases: Medical strategy analysis

   1. Kodolitsch, Yskert
   2. Kutsche, K

   2017 - Forschungsinformationssystem des UKE
3. Structure-function-behavior relationship in estrogen-induced synaptic plasticity

   1. Vierk, R
   2. Bayer, J
   3. Freitag, S
   4. Muhia, M
   5. Kutsche, K
   6. Wolbers, T
   7. Kneussel, M

   2015 - Forschungsinformationssystem des UKE
4. Branchio-otic syndrome caused by a genomic rearrangement: clinical findings and molecular cytogenetic studies in a patient with a pericentric inversion of chromosome 8

   1. Schmidt, T
   2. Bierhals, T
   3. Kortüm, F
   4. Bartels, I
   5. Liehr, T
   6. Burfeind, P
   7. Shoukier, M

   2014 - Forschungsinformationssystem des UKE
5. Dysfunction of SHANK2 and CHRNA7 in a patient with intellectual disability and language impairment supports genetic epistasis of the two loci

   1. Chilian, B
   2. Abdollahpour, H
   3. Bierhals, T
   4. Haltrich, I
   5. Fekete, G
   6. Nagel, I
   7. Rosenberger, G

   2013 - Forschungsinformationssystem des UKE