You are here:
- Homepage
- Diseases & therapies
- Special consultation hours - neuromuscular diseases
- Exome/Panel diagnostics
- Intellectual disability
- Epilepsy
- Skeletal diseases and unclear skeletal phenotypes
- Kidney diseases
- Neuromuscular diseases
- Marfan syndrome, EDS & other connective tissue diseases
- Noonan syndrome and hypertrophic cardiomyopathy
- Lipodystrophy
- Neuroendocrine tumours
- Hypertension
- Paediatric lung diseases
- Paediatric lung diseases
- Paediatric lung diseases
- Other syndromic diseases
- Array CGH diagnostics
- Registration & general information about consultations
- Special consultation hours - eye diseases
- Special consultation hours - paediatric developmental disorders
- Special consultation hours - Marfan syndrome
- Special consultation hours - neuromuscular diseases
- Special consultation hours - kidney diseases
- Special consultation hours - prenatal diagnostics
- Special consultation hours - skeletal diseases
- Special consultation hours - hereditary tumour diseases
Contact
Univ. Prof. Brunhilde Wirth, PhD
Specialist in Human Genetics, GfH (German Society of Human Genetics)
European Clinical Laboratory Geneticist
Email brunhilde.wirth@uk-koeln.de
Dr. Mert Karakaya
Medical Specialist in Human Genetics
E-Mail mert.karakaya@uk-koeln.de
Appointments
Appointments are made daily by arrangement at the Medical Health Center (MVZ) of the University of Cologne or in the Institute’s Outpatient Clinic.
Register for consultation at MVZ
Telephone +49 221 478-86837
Fax +49 221 478-1460228
E-Mail mvz-humangenetik@uk-koeln.de
Register for consultation at the Outpatient Center
Telephone +49 221 478-86214
Fax +49 221 478-1460466
E-Mail humangenetik@uk-koeln.de