2 Einträge gefunden

1. Compound heterozygous GATA5 mutations in a girl with hydrops fetalis, congenital heart defects and genital anomalies

   1. Hempel, Maja
   2. Casar Tena, Teresa
   3. Diehl, Thilo
   4. Burczyk, Martina S
   5. Strom, Tim M
   6. Kubisch, Christian
   7. Philipp, Melanie

   2017 - Forschungsinformationssystem des UKE
2. 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