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Article

Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure.

Fertility and sterility - 1 Apr 2011

McGuire Megan M, Bowden Wayne, Engel Natalie J, Ahn Hyo Won, Kovanci Ertug, Rajkovic Aleksandar

Abstract excerpt

OBJECTIVE: To analyze DNA from women with premature ovarian failure (POF) for genome-wide copy-number variations (CNVs), focusing on novel autosomal microdeletions. DESIGN: Case-control genetic association study. SETTING: Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas. PATIENT(S): Of 89 POF patients, eight experienced primary amenorrhea and 81 exhibited secondary amenorrhea...

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Identifiers

PMID: 21256485
DOI: 10.1016/j.fertnstert.2010.12.052
PMCID: PMC3062633

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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