2 Einträge gefunden

1. 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
2. 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