3 Einträge gefunden

1. 16p13.11 microdeletion uncovers loss-of-function of a MYH11 missense variant in a patient with megacystis-microcolon-intestinal-hypoperistalsis syndrome

   1. Kloth, Katja
   2. Renner, Sina
   3. Burmester, Gunter
   4. Steinemann, Doris
   5. Pabst, Brigitte
   6. Lorenz, Birgit
   7. Simon, Ronald

   2019 - Forschungsinformationssystem des UKE
2. Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients

   1. Renner, Sina
   2. Schüler, Helke
   3. Alawi, Malik
   4. Kolbe, Verena
   5. Rybczynski, Meike
   6. Woitschach, Rixa
   7. Sheikhzadeh, Sara

   2019 - Forschungsinformationssystem des UKE
3. Genetische und funktionelle Analysen zu Ursachen und Pathogenese von erblichen Aortenerkrankungen, Genetic and functional analyses of causes and pathogenesis of hereditary aortic diseases

   1. Renner, Sina

   2019 - E-Dissertationen der UHH - frei zugänglich