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Article

Intrauterine phenotypic features associated with 16p11.2 recurrent microdeletions.

Prenatal diagnosis - 1 May 2018

Lin Shaobin, Shi Shanshan, Zhou Yi, Ji Yuanjun, Huang Peizhi, Wu Jianzhu, Chen Baojiang, Luo Yanmin

Abstract excerpt

OBJECTIVE: To investigate the detection rate of 16p11.2 recurrent microdeletions in fetuses with abnormal ultrasound findings and determine the common abnormal ultrasound findings in fetuses carrying the deletion. METHODS: This study reviewed 2262 consecutive fetuses with abnormal ultrasound findings who underwent prenatal chromosomal microarray analysis between October 2014 and December 2016. Cases carrying the...

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PMID: 29514395
DOI: 10.1002/pd.5245

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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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