Frequency / statistic
Signs & symptoms
1 supporting source
confidence 80%
novelty 60%
In one study of Müllerian aplasia, 4/63 cases (6 per cent) were linked to a 17q12 microdeletion
A source reports “63 cases” in the context of mullerian gu: “In one study of Müllerian aplasia, 4/63 cases (6 per cent) were linked to a 17q12 microdeletion.”
How this was derived
Numbers are quoted verbatim from the source; check the source before quoting onward.
Generated 2026-11-13, last changed
today. Dedup key freq:63 cases.
The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.
Evidence (1 quote)
In one study of Müllerian aplasia, 4/63 cases (6 per cent) were linked to a 17q12 microdeletion.
Supporting documents (1)
| Document | Source | Published | Seen | Relevance |
|---|---|---|---|---|
| 17q12 microdeletions (rarechromo.org patient leaflet) | patient_org | - | today | 1.00 |