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Article

A genome-wide screen for copy number alterations in an adolescent pilot cohort with müllerian anomalies.

Fertility and sterility - 1 Feb 2015

Murry Jaclyn B, Santos Xiomara M, Wang Xiaoling, Wan Ying-Wooi, Van den Veyver Ignatia B, Dietrich Jennifer E

Abstract excerpt

OBJECTIVE: To examine whether pathogenic copy number changes (CNCs) can be identified in deoxyribonucleic acid from females with different classes of müllerian anomalies. DESIGN: We conducted array-based copy number variant (CNV) analysis using an oligonucleotide array from deoxyribonucleic acid in 12 adolescent females with various müllerian anomalies. SETTING: University-affiliated tertiary care institution....

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 25492685
DOI: 10.1016/j.fertnstert.2014.10.044
PMCID: PMC4476902

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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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