Marfan syndrome and type 1 fibrillinopathies: Heidelberg University Hospital

Heidelberg University Hospital

Search

Heidelberg University Hospital

Welcome
Our Team
- Our Team
- Contact
For Patients
For Patients
Genetic Out-Patient Clinic
- Genetische Poliklinik
  
  FAQ
For Physicians
For Physicians
- Requisition Forms
- Consil
- Directory of Services
Research
Research
- Section Nephrogenetics (AG Simons)
- Seniorprofessorship Prof. Rappold
- Molecular Neurogenetics (AG Berkel)
- Cardiogenetics (AG Hoffmann)
- Neurogastrogenetics
  
  nCounter Core Facility
- Transcriptional regulation in developmental disorders (AG Laugsch)
- Genetics of neurodevelopmental disorders (AG Schaaf)
- Mouse models for neurodevelopmental disorders
- Research in our Diagnostic Laboratories
- Publications
Diagnostics
Diagnostics
- Molecular Genetics Laboratory
- Molecular-cytogenetic laboratory (FISH)
  
  Range of methods
- Cytogenetics Laboratory
- MRD Laboratory
- Quality Management
Teaching
Teaching
- Colloquium
News

Institute of Human Genetics

Institute of Human… For Physicians Directory of… Marfan syndrome and…

* non-accredited examination systems

EN