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Article

Complex X chromosome rearrangement delineated by array comparative genome hybridization in a woman with premature ovarian insufficiency.

Fertility and sterility - 1 Jun 2011

Ochalski Melanie E, Engle Natalie, Wakim Anthony, Ravnan Britt J, Hoffner Lori, Rajkovic Aleksandar, Surti Urvashi

Abstract excerpt

OBJECTIVE: To investigate candidate genes affected by a complex X chromosome rearrangement that may play a role in the diagnosis of spontaneous premature ovarian insufficiency (POI). DESIGN: Prospective cytogenetic analysis, fluorescence in situ hybridization (FISH) analysis and oligonucleotide a...

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Share to Chromosome Breakpoints
Share to Chromosome Duplication
Share to Chromosomes, Human, X

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Comparative Genomic Hybridization

Share to Gene Rearrangement

Share to Ovulation

Share to Primary Ovarian Insufficiency

Share to Translocation, Genetic

Source

Identifiers

PMID: 21530964
DOI: 10.1016/j.fertnstert.2011.03.082

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21530964-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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