2 Einträge gefunden

1. Exome sequencing identifies a novel heterozygous TGFB3 mutation in a disorder overlapping with Marfan and Loeys-Dietz syndrome

   1. Kuechler, Alma
   2. Altmüller, Janine
   3. Nürnberg, Peter
   4. Kotthoff, Stefan
   5. Kubisch, Christian
   6. Borck, Guntram

   2015 - Forschungsinformationssystem des UKE
2. Female carriers of X-chromosomal adrenoleukodystrophy: a major differential diagnosis in progressive myelopathy.

   1. Guettsches, Anne-Katrin
   2. Kuechler, Alma
   3. Gal, Andreas
   4. Schmitz, Werner
   5. Tegenthoff, Martin
   6. Vorgerd, Matthias

   2010 - Forschungsinformationssystem des UKE