17q12, explained for kidsdeletion syndrome · static snapshot
Adults Scientists Kids EN NL
Everything here was found on the internet and put together with help from a computer program that reads and writes (AI). It is here so you can learn — it is not the final word. Always check the real source. Read the whole notice
A new article Genes and families 1 supporting source confidence 97% novelty 75%

A familial case report of 17q12 recurrent deletion syndrome: clinical and molecular characterization.

1664-2392 17 2026 Frontiers in endocrinology Front Endocrinol (Lausanne) A familial case report of 17q12 recurrent deletion syndrome: clinical and molecular characterization.

More a new article

How this was derived

Indexed from **pubmed** on 2026-11-12 (relevance 1.00, tier peer_reviewed).

Generated 2026-11-14, last changed today. Dedup key newdoc:15. 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)

A familial case report of 17q12 recurrent deletion syndrome: clinical and molecular characterization. peer_reviewed · published 2026-01-01 · live page
1819047 1819047 1819047 10.3389/fendo.2026.1819047 This article presents the first reported familial case of 17q12 recurrent deletion syndrome in Russia, involving a female patient with diabetes and her daughter diagnosed with atypical autism without intellectual disability.

Supporting documents (1)

StorySourcePublishedSeenRelevance
A familial case report of 17q12 recurrent deletion syndrome: clinic... pubmed 2026-01-01 yesterday 1.00