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Article

A 15q25.2 microdeletion phenotype for premature ovarian failure in a Chinese girl: a case report and review of literature.

BMC medical genomics - 7 Sept 2020

Chen Zhen, Chen Hong, Yuan Ke, Wang Chunlin

Abstract excerpt

BACKGROUND: Proximal microdeletions on chromosome 15q25.2 are very rare, and are associated with neurodevelopmental delay, inguinal hernia, chest deformities, and anemia. The minimum length missed so far is 1.4 Mb. However, there were no cases reported till date on microdeletions at position q25.2 on chromosome 15 with premature ovarian failure (POF). CASE PRESENTATION: We herein reported a POF case characterized...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 32894148
DOI: 10.1186/s12920-020-00787-w
PMCID: PMC7487592

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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