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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

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

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How this was derived

Indexed from **openalex** on 2026-11-13 (relevance 1.00, tier peer_reviewed).

Generated 2026-11-13, last changed yesterday. Dedup key newdoc:522. 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 2026-05-12 · live page
A familial case report of 17q12 recurrent deletion syndrome: clinical and molecular characterization 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)

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A familial case report of 17q12 recurrent deletion syndrome: clinic... openalex 2026-05-12 yesterday 1.00