New publication
What it is
1 supporting source
confidence 97%
novelty 75%
17q12 microdeletion syndrome - Rare Awareness Rare Education Portal
17q12 microdeletion syndrome is a chromosomal condition in which a small part of chromosome 17 is missing (deleted). 1 This small deletion, also known as a microdeletion, occurs at a location on chromosome 17 called 17q12.
How this was derived
Indexed from **web** on 2026-11-13 (relevance 1.00, tier curated).
Generated 2026-11-13, last changed
today. Dedup key newdoc:566.
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Evidence (1 quote)
17q12 microdeletion syndrome - Rare Awareness Rare Education Portal
curated
· published 2025-08-01
· live page
In rare cases, the deletion was inherited from a parent in an autosomal dominant manner (there is a 50% chance that an affected parent will pass it to each of their children).
Supporting documents (1)
| Document | Source | Published | Seen | Relevance |
|---|---|---|---|---|
| 17q12 microdeletion syndrome - Rare Awareness Rare Education Portal | web | 2025-08-01 | today | 1.00 |