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Article

De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency.

BJOG : an international journal of obstetrics and gynaecology - 1 Jan 2009

Law L W, Lau T K, Fung T Y, Leung T Y, Wang C C, Choy K W

Abstract excerpt

OBJECTIVE: We investigated the application of high-resolution microarray-based comparative genomic hybridisation (array CGH) on a fetus showing increased nuchal translucency (NT). DESIGN: Case study. SETTING: Tertiary referral obstetrics unit. SAMPLE: Pregnant woman attended the antenatal clinic. METHODS: Conventional karyotyping and genetic test was carried out for the alpha-globin gene. High-resolution array...

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PMID: 19018765
DOI: 10.1111/j.1471-0528.2008.01948.x

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

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