Universitätsklinikum Essen Institut für Humangenetik
40 capabilities
Accredited since October 2025
Verified Apr 2026
One of 3,039 in Germany
Details
Virchowstraße 171
Essen 45147 , Germany
Essen 45147 , Germany
Accreditation
Active
DAkkS
D-ML-18383-04-01
Conducts molecular and cytogenetic human genetic testing using PCR, sequencing, and multiplex ligation-dependent probe amplification methods on DNA and tissue samples.
Accreditation Details
Accreditation Body
DAkkS
Number
D-ML-18383-04-01
Status
ActiveSince
23 October 2025
Accreditation is granted under EU Regulation 765/2008 and assessed against ISO/IEC 17025. Data sourced from official DAkkS records.
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Test Capabilities (40)
| Standard Reference | Description | Category |
|---|---|---|
| Angeborener Chromosomensatz | angeborener Chromosomensatz | Biocompatibility (ISO 10993) |
| Whole Exome Sequenzierung (WES) | Whole Exome Sequenzierung (WES) | Elemental Analysis |
| Whole Genome Sequenzierung | Whole Genome Sequenzierung | Elemental Analysis |
| (Clinical Exome) | (Clinical Exome) | Molecular Diagnostics / PCR |
| (Hearing impairment) | (Hearing impairment) | Molecular Diagnostics / PCR |
| (ICR1, ICR2) in 11p15; (MEG3 ) in | (ICR1, ICR2) in 11p15; (MEG3 ) in | Molecular Diagnostics / PCR |
| (MAGEL2) Chromosom 15q12 | (MAGEL2) Chromosom 15q12 | Molecular Diagnostics / PCR |
| (SNRPN, MAGEL2 ) in 15q11q13 | (SNRPN, MAGEL2 ) in 15q11q13 | Molecular Diagnostics / PCR |
| 14p32; (GRB10, MEST) in 7p12 | 14p32; (GRB10, MEST) in 7p12 | Molecular Diagnostics / PCR |
| 7q32 | 7q32 | Molecular Diagnostics / PCR |
| Chromosom 11p15.5; (UBE3A ) | Chromosom 11p15.5; (UBE3A ) | Molecular Diagnostics / PCR |
| Chromosom 15 | Chromosom 15 | Molecular Diagnostics / PCR |
| Chromosom 7, 11, 14 | Chromosom 7, 11, 14 | Molecular Diagnostics / PCR |
| Chromosom15q11.2 | Chromosom15q11.2 | Molecular Diagnostics / PCR |
| Differentialdiagnosen (AS DD) | Differentialdiagnosen (AS DD) | Molecular Diagnostics / PCR |
| Gendosisanalyse | Gendosisanalyse | Molecular Diagnostics / PCR |
| Gendosisanalyse (BE3A, SHOX ) | Gendosisanalyse (BE3A, SHOX ) | Molecular Diagnostics / PCR |
| Genet. Veränderung bei | Genet. Veränderung bei | Molecular Diagnostics / PCR |
| Genetische Veränderung bei | Genetische Veränderung bei | Molecular Diagnostics / PCR |
| Genmutationen | Laktoseintoleranz Genmutationen | Molecular Diagnostics / PCR |
| Genotypisierung an multiplen Loci | Genotypisierung an multiplen Loci | Molecular Diagnostics / PCR |
| Genotypisierung von | Genotypisierung von | Molecular Diagnostics / PCR |
| Identifikation des parentalen Allels | Identifikation des parentalen Allels | Molecular Diagnostics / PCR |
| Imprintingerkrankung: | Imprintingerkrankung: Gendosis- | Molecular Diagnostics / PCR |
| Intelligenzminderung | Syndrom der Intelligenzminderung | Molecular Diagnostics / PCR |
| Lungenfibrose | Lungenfibrose | Molecular Diagnostics / PCR |
| Mikrosatellitenmarkern im Bereich | Mikrosatellitenmarkern im Bereich | Molecular Diagnostics / PCR |
| Mutationsanalyse (CDKN1C) | Mutationsanalyse (CDKN1C) | Molecular Diagnostics / PCR |
| Mutationsanalyse und | Mutationsanalyse und | Molecular Diagnostics / PCR |
| Segregationsanalyse | Segregationsanalyse | Molecular Diagnostics / PCR |
| Syndrom - Differentialdiagnosen | Syndrom - Differentialdiagnosen | Molecular Diagnostics / PCR |
| Tumorerkrankung: Analyse auf | Tumorerkrankung: Analyse auf | Molecular Diagnostics / PCR |
| Verlust eines Chromosoms 3 | Verlust eines Chromosoms 3 | Molecular Diagnostics / PCR |
| des RB1 -Gen | des RB1 -Gen | Molecular Diagnostics / PCR |
| (Monozygotie; Ausschluss | (Monozygotie; Ausschluss | Other |
| (WGS) | (WGS) | Other |
| SHFYNG DD) | SHFYNG DD) | Other |
| inkl. Schaaf-Yang-Syndrom (PWS | inkl. Schaaf-Yang-Syndrom (PWS | Other |
| mütterlicher Kontamination) | mütterlicher Kontamination) | Other |
| Gerichtete NGS-Panel-Analyse | Gerichtete NGS-Panel-Analyse | Spectroscopy (XRF, ICP, AAS) |