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Article

Microarray detection of a de novo der(X)t(X;11)(q28;p13) in a girl with premature ovarian failure and features of Beckwith-Wiedemann syndrome.

Journal of human genetics - 1 Jan 2006

Han Jin-Yeong, Shin Ji-Hyun, Han Myong-Seok, Je Goo-Hwa, Shaffer Lisa G

Abstract excerpt

We report an 18-year-old girl with premature ovarian failure (POF), tall stature, and urinary incontinence. Chromosome studies including array comparative genomic hybridization showed that she was the carrier of an unbalanced de novo translocation between the X chromosome and chromosome 11, resul...

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Source

Identifiers

PMID: 16708166
DOI: 10.1007/s10038-006-0409-2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-16708166-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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