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Article

Genetic effects of a 13q31.1 microdeletion detected by noninvasive prenatal testing (NIPT).

International journal of clinical and experimental pathology - 1 Jan 2014

Jia Yifang, Zhao Heyong, Shi Donghong, Peng Wen, Xie Luwen, Wang Wei, Jiang Fuman, Zhang Hongyun, Wang Xietong

Abstract excerpt

Microdeletions of chromosome 13q31.1 are relatively rare. These types of deletions may cause different genetic effects on genotypes and/or phenotypes. There are several ways to detect microdeletions; noninvasive prenatal testing (NIPT) is the newest detection method. In this study, we aimed to investigate the genetic effects of a 13q31.1 microdeletion detected by NIPT and to reconfirm the feasibility of this...

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Identifiers

PMID: 25400788
PMCID: PMC4230093

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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