Reply within 24 hours
New enquiries are usually triaged within one day so that the instructing party quickly knows feasibility and the next step.
The process is designed for rapid preliminary review, a clear document checklist and a transparent workflow.
Short outline of the instructing party, question, deadline and file volume.
Assessment of whether the case is suitable for human genetics review and can be clearly scoped.
Alignment of scope, records needed, timetable and expected output format.
Structured review with a clear conclusion and defined reasoning path.
A good starting structure saves time. For an initial review, only a few but clearly defined items are usually required.
Preferably quoted directly from the court order, insurer letter or internal request.
Essential for feasibility and prioritisation.
Laboratory reports, outside findings, segregation data or indications of previous analyses.
Medical reports, course summaries, functional descriptions and relevant ancillary findings.
New enquiries are usually triaged within one day so that the instructing party quickly knows feasibility and the next step.
Before work starts, it is clarified whether a full report, supplemental opinion or focused variant assessment is the appropriate format.
Missing records or unclear points are identified precisely to avoid unnecessary delays.
After receipt of the enquiry, a short specialist pre-review is performed. This clarifies whether the question is suitable for human genetics review, which records are required for a robust opinion and whether the available material is already sufficient or should be supplemented.
Once the mandate is accepted, the records and findings are reviewed in a structured manner, always oriented to the core question. The result is a linguistically clear, methodologically transparent opinion or full report that is directly usable for the instructing party.
For a new case, a brief email with the question, deadline, approximate file volume and available genetic findings is sufficient.