4 Einträge gefunden

1. Mutations in NDUFB11, Encoding a Complex I Component of the Mitochondrial Respiratory Chain, Cause Microphthalmia with Linear Skin Defects Syndrome

   1. van Rahden, Vanessa A
   2. Fernandez-Vizarra, Erika
   3. Alawi, Malik
   4. Brand, Kristina
   5. Fellmann, Florence
   6. Horn, Denise
   7. Zeviani, Massimo

   2015 - Forschungsinformationssystem des UKE
2. Clinical spectrum of females with HCCS Mutation: from no clinical signs to a neonatal lethal form of the microphthalmia with linear skin defects (MLS) syndrome

   1. van Rahden, Vanessa A
   2. Rau, Isabella
   3. Fuchs, Sigrid
   4. Kosyna, Friederike K
   5. de Almeida, Hiram Larangeira
   6. Fryssira, Helen
   7. Isidor, Bertrand

   2014 - Forschungsinformationssystem des UKE - frei zugänglich
3. Evidence of Germline Mosaicism for a Novel BCOR Mutation in Two Indian Sisters with Oculo-Facio-Cardio-Dental Syndrome

   1. Danda, Sumita
   2. van Rahden, Vanessa A
   3. John, Deepa
   4. Paul, Padma
   5. Raju, Renu
   6. Koshy, Santosh
   7. Kutsche, Kerstin

   2014 - Forschungsinformationssystem des UKE
4. The Legionella effector RidL inhibits retrograde trafficking to promote intracellular replication

   1. Finsel, Ivo
   2. Ragaz, Curdin
   3. Hoffmann, Christine
   4. Harrison, Christopher F
   5. Weber, Stephen
   6. van Rahden, Vanessa A
   7. Johannes, Ludger

   2013 - Forschungsinformationssystem des UKE