4 Einträge gefunden

1. BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells

   1. Lessel, Davor
   2. Gehbauer, Christina
   3. Bramswig, Nuria C
   4. Schluth-Bolard, Caroline
   5. Venkataramanappa, Sathish
   6. van Gassen, Koen L I
   7. Hempel, Maja

   2018 - Forschungsinformationssystem des UKE
2. LYRM7 - associated complex III deficiency: A clinical, molecular genetic, MR tomographic, and biochemical study

   1. Hempel, Maja
   2. Kremer, Laura S
   3. Tsiakas, Konstantinos
   4. Alhaddad, Bader
   5. Haack, Tobias B
   6. Löbel, Ulrike
   7. Feichtinger, René G

   2017 - Forschungsinformationssystem des UKE
3. Exome Sequencing is a Valuable Approach in Critically Ill Patients with Suspected Monogenic Disease: Diagnosis of X-linked Centronuclear Myopathy in Preterm Twins

   1. Johannsen, Jessika
   2. Hempel, Maja
   3. Diehl, Thilo
   4. Haack, Tobias B
   5. Denecke, Jonas

   2017 - Forschungsinformationssystem des UKE - frei zugänglich
4. De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment

   1. Hempel, Maja
   2. Cremer, Kirsten
   3. Ockeloen, Charlotte W
   4. Lichtenbelt, Klaske D
   5. Herkert, Johanna C
   6. Denecke, Jonas
   7. Haack, Tobias B

   2015 - Forschungsinformationssystem des UKE