ScopeMGZ - Medizinisch Genetisches Zentrum MVZ Holinski-Feder, Abicht und Neuhann Partnerschaft von Fachärztinnen für Humangenetik mbB
Official name: MGZ - Medizinisch Genetisches Zentrum MVZ Prof. Dr. Holinski-Feder, Prof. Dr. Abicht und Dr. Neuhann Partnerschaft von Fachärztinnen für Humangenetik mbB
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Details
München 80335 , Germany
Accreditation
Specialises in molecular human genetics and cytogenetics with flexible scope for procedure modification and development. Testing includes PCR, Sanger sequencing, and multiplex ligation-dependent probe amplification analysis on blood, tissue, and cultured cell samples.
Accreditation Details
Accreditation Body
DAkkS
Number
D-ML-13242-01-00
Status
ActiveSince
12 June 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 (38)
| Standard Reference | Description | Category |
|---|---|---|
| Angeborener Chromosomensatz | angeborener Chromosomensatz | Biocompatibility (ISO 10993) |
| DPYD-Genvarianten | DPYD-Genvarianten | Biocompatibility (ISO 10993) |
| ATXN2-Repeat | ATXN2-Repeat | Biological / Microbiological |
| BRAF | p.T790M, EGFR p.L858R, BRAF | Biological / Microbiological |
| EGFR | EGFR exon 19 deletions, EGFR | Biological / Microbiological |
| (OMIM300005) | (OMIM300005) | Molecular Diagnostics / PCR |
| (OMIM309550) | (OMIM309550) | Molecular Diagnostics / PCR |
| 13, 18, 21, X, Y | 13, 18, 21, X, Y | Molecular Diagnostics / PCR |
| Aneuploidien (NIPT) | Aneuploidien (NIPT) | Molecular Diagnostics / PCR |
| Aneuploidien, seltene autosomale | Aneuploidien, seltene autosomale | Molecular Diagnostics / PCR |
| C9orf72 -Repeat (OMIM614260) | C9orf72 -Repeat (OMIM614260) | Molecular Diagnostics / PCR |
| Chromosomensatz | Konstitutioneller Chromosomensatz | Molecular Diagnostics / PCR |
| Chromosomensatz | Hemizygoter Chromosomensatz | Molecular Diagnostics / PCR |
| D4Z4 Repeat (DUX4 Gen) | D4Z4 Repeat (DUX4 Gen) | Molecular Diagnostics / PCR |
| DIN EN 602 (2004-07) | DQB1*0602 | Molecular Diagnostics / PCR |
| Deletions/Duplikationsanalyse | Deletions/Duplikationsanalyse | Molecular Diagnostics / PCR |
| Duplikationen und Deletionen > | Duplikationen und Deletionen > | Molecular Diagnostics / PCR |
| EPCAM, MLH1, MSH2, MSH6, PMS2 | EPCAM, MLH1, MSH2, MSH6, PMS2 | Molecular Diagnostics / PCR |
| Faktor VII-Mangel | Faktor VII-Mangel | Molecular Diagnostics / PCR |
| Fragiles X Syndrom: FMR1 | Fragiles X-Syndrom: FMR1 | Molecular Diagnostics / PCR |
| Kombinierter Lipasemangel | Kombinierter Lipasemangel | Molecular Diagnostics / PCR |
| MB für alle Autosomen, geschlechtschromosomale | MB für alle Autosomen, geschlechtschromosomale | Molecular Diagnostics / PCR |
| MECP2-Gen, RETT Syndrom | MECP2-Gen, RETT Syndrom | Molecular Diagnostics / PCR |
| Mangel | Ornithin-Transcarbamylase-Mangel | Molecular Diagnostics / PCR |
| MeCP2; Rett-Syndrom | MeCP2; Rett-Syndrom | Molecular Diagnostics / PCR |
| Nachweis somatischer Varianten | Nachweis somatischer Varianten | Molecular Diagnostics / PCR |
| PMP22 (OMIM601097) | PMP22 (OMIM601097) | Molecular Diagnostics / PCR |
| Partieller konstitutioneller | Partieller konstitutioneller | Molecular Diagnostics / PCR |
| Trisomie 13, 18, 21, partielle | Trisomie 13, 18, 21, partielle | Molecular Diagnostics / PCR |
| V.a. Rasopathie: KRAS c.35G>A, p.(Gly12Asp) | V.a. Rasopathie: KRAS c.35G>A, p.(Gly12Asp) | Molecular Diagnostics / PCR |
| Whole Exome Sequencing | Whole Exome Sequencing | Molecular Diagnostics / PCR |
| p.V600E, KRAS p.G12/p.G13 | p.V600E, KRAS p.G12/p.G13 | Molecular Diagnostics / PCR |
| FSHD1/FSHD2 Methylierung: | FSHD1/FSHD2 Methylierung: | Other |
| Frontotemporale Demenz, FTD-ALS: | Frontotemporale Demenz, FTD-ALS: | Other |
| HNPCC / Lynch-Syndrom ID.099: | HNPCC / Lynch-Syndrom ID.099: | Other |
| Methylierungsstatus und | Methylierungsstatus und | Other |
| Neuropathie, demyelinisierend: | Neuropathie, demyelinisierend: | Other |
| Prader Willi Syndrom | Prader-Willi-Syndrom: | Other |
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