17q12 Knowledge Basedeletion syndrome · static snapshot
Adults Scientists Kids EN NL
All content was collected from public internet sources and processed with the help of AI/LLM software. This site is informative only — do not draw conclusions; verify with the original sources. Full disclaimer
New publication Genes & inheritance 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 new publication

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)

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