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Article

Adverse Perinatal and Early Life Outcomes following 15q11.2 CNV Diagnosis.

Genes - 23 Sept 2021

Chu Fu-Chieh, Shaw Steven W, Lee Chien-Hong, Lo Liang-Ming, Hsu Jenn-Jeih, Hung Tai-Ho

Abstract excerpt

The copy number variation (CNV) of 15q11.2, an emerging and common condition observed during prenatal counseling, is encompassed by four highly conserved and non-imprinted genes-TUBGCP5, CYFIP1, NIPA1, and NIPA2-which are reportedly related to developmental delays or general behavioral problems. We retrospectively analyzed 1337 samples from genetic amniocentesis for fetal CNV using microarray-based comparative...

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Identifiers

PMID: 34680874
DOI: 10.3390/genes12101480
PMCID: PMC8535766

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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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