ScopeKlinikum der Julius-Maximilians-Universität Würzburg (Universitätsklinikum Würzburg) Institut für Klinische Genetik und Genommedizin
15 capabilities
Accredited since October 2025
Verified Oct 2026
One of 3,209 in Germany
Send one structured enquiry and we chase the reply for you. No cold email, no chasing.
Details
Am Hubland
Würzburg 97074 , Germany
Würzburg 97074 , Germany
Accreditation
Active
DAkkS
D-ML-13450-02-01
www.ukw.de/klinische-genetik-und-genommedizin/d...
Prefer to enquire through us? Send an enquiry
Specializes in molecular human genetics diagnostics, offering testing for inherited genetic disorders through techniques including bisulfite conversion, PCR, Sanger sequencing, and molecular karyotypization on blood and DNA samples.
Accreditation Details
Accreditation Body
DAkkS
Number
D-ML-13450-02-01
Status
ActiveSince
01 October 2025
Accreditation is granted under EU Regulation 765/2008 and assessed against ISO/IEC 17025. Data sourced from official DAkkS records.
Download Scope PDFAdditional scope documents
Test Capabilities (15)
| Standard Reference | Description | Category |
|---|---|---|
| Curschmann-Steinert (DMPK) | Curschmann-Steinert (DMPK) | Food Safety Testing |
| Fazio-skapulo-humerale | Fazio-skapulo-humerale | Food Safety Testing |
| Hämophilie A (F8, Inversion 1) | Hämophilie A (F8, Inversion 1) | Food Safety Testing |
| Hörstörungs-Panel; SNV | Hörstörungs-Panel; SNV | Food Safety Testing |
| Muskeldystrophie / FSHD1 (D4Z4) | Muskeldystrophie / FSHD1 (D4Z4) | Food Safety Testing |
| Myopathie-Panel; SNV | Myopathie-Panel; SNV | Food Safety Testing |
| Spinale Muskelatrophie, SMA I,II,III | Spinale Muskelatrophie, SMA I,II,III | Food Safety Testing |
| Whole Exome, SNV | Whole Exome, SNV | Food Safety Testing |
| (SMN1) | SMN1-Gen (SMN1) | Molecular Diagnostics / PCR |
| Hereditäre | Hereditäre | Molecular Diagnostics / PCR |
| Hypophosphatasie (ALPL) | Hypophosphatasie (ALPL) | Molecular Diagnostics / PCR |
| Muskeldystrophie, FSHD2, (SMCHD1, D4Z4-Methylierung); SNV | Muskeldystrophie, FSHD2, (SMCHD1, D4Z4-Methylierung); SNV | Molecular Diagnostics / PCR |
| Myotone Dystrophie Typ 1 / M. | Myotone Dystrophie Typ 1 / M. | Molecular Diagnostics / PCR |
| Tumorprädispositionssyndrome (TruSight Hereditary Cancer-Panel); SNV, CNV | Tumorprädispositionssyndrome (TruSight Hereditary Cancer-Panel); SNV, CNV | Molecular Diagnostics / PCR |
| Whole Genome, SNV | Whole Genome, SNV | Molecular Diagnostics / PCR |
Send an Enquiry
Request a quote, ask about capacity, or discuss your testing requirements directly with this lab.