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Article

Clinical and genetic analysis of a phenotypically normal three-generation family carrying 10.884 Mb deletions at 13q21.1q21.32.

Taiwanese journal of obstetrics & gynecology - 1 Jul 2026

Wang Xiao-Lin, Niu Lin-Yuan, Wang Yu-Jiao, Zhang Chun-Xiao, Wang Yu-Juan, Cui Qian, Lan Xin-Qiang

Abstract excerpt

OBJECTIVE: Patients with variations exhibiting abnormal phenotypes or no significant clinical signs offer crucial insights into our genome's complexities. To help determine the pathogenicity of 13q21.1q21.32 deletion, we reported four patients in a family carrying this variation. CASE REPORT: Our study identified a family of four patients harboring a deletion of approximately 10.884 Mb spanning 13q21.1 to q21.32,...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 42362274
DOI: 10.1016/j.tjog.2024.11.016

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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