17q12, explained for kidsdeletion syndrome · static snapshot
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Something new reported Kidneys and diabetes 1 supporting source confidence 97% novelty 90%

Someone reported something new: A familial case report of 17q12 recurrent deletion syndrome: clinical and molecular characterization This arti…

A source describes a new or expanded observation: “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”

More something new reported

How this was derived

Flagged by novelty language (“for the first time”, “expands the phenotype”, …) in openalex.

Generated 2026-11-13, last changed today. Dedup key expansion:80c9c5. 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