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- Diseases & Therapies
- Single gene diagnostics
- Single gene diagnostics
- Genome sequencing pilot project
- Exom- and Panel diagnostics
- Array CGH diagnostics
- Registration & general information on consultation hours
- Special consultation hours for eye diseases
- Special consultation hours for child development disorders
- Special consultation for Marfan syndrome
- Special consultation hours for neuromuscular diseases
- Special consultation for kidney diseases
- Special consultation hours for prenatal diagnostics
- Special consultation hours - skeletal diseases
- Special consultation hours for hereditary tumor diseases
Single gene diagnostics
Even with the advent of high-throughput genetic analysis, targeted analysis of a single gene or gene segment is still the most useful approach for certain questions. In general, these analyses continue to be performed using Sanger sequencing. Use the menu on the left or our request form for an overview of our diagnostic services.
Depending on the scope and urgency of the request, the test wait period ranges from a few days to a maximum of 6 weeks.
Contact
Diagnostics office
Telephone +49 221 478-86811
Fax +49 221 478 1460228
E-Mail humangenetik@uk-koeln.de