A familial case report of 17q12 recurrent deletion syndrome: clinical and molecular characterization.
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| Title: | A familial case report of 17q12 recurrent deletion syndrome: clinical and molecular characterization. |
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| Authors: | Dvoryanchikov YV; Endocrinology Research Centre, Moscow, Russia., Khusainova RI; Endocrinology Research Centre, Moscow, Russia., Minniakhmetov IR; Endocrinology Research Centre, Moscow, Russia., Salakhov RR; Endocrinology Research Centre, Moscow, Russia., Smirnov KV; Endocrinology Research Centre, Moscow, Russia., Ibragimova SA; Endocrinology Research Centre, Moscow, Russia., Golodnikov II; Endocrinology Research Centre, Moscow, Russia., Sechko EA; Endocrinology Research Centre, Moscow, Russia., Dobreva EA; Endocrinology Research Centre, Moscow, Russia., Mokrysheva NG; Endocrinology Research Centre, Moscow, Russia. |
| Source: | Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2026 May 12; Vol. 17, pp. 1819047. Date of Electronic Publication: 2026 May 12 (Print Publication: 2026). |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101555782 Publication Model: eCollection Cited Medium: Print ISSN: 1664-2392 (Print) Linking ISSN: 16642392 NLM ISO Abbreviation: Front Endocrinol (Lausanne) Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1664-2392 |
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| DOI: | 10.3389/fendo.2026.1819047 |
