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Article

Microarray Application in Newborns With Multiple Congenital Anomalies: Genotype-Phenotype Correlation.

Birth defects research - 1 Jul 2025

Keçeci Ramazan, Keçeci Hayriye Nermin, Başdemirci Müşerref

Abstract excerpt

BACKGROUND: Microarray is considered the first step in the diagnostic test in patients with multiple congenital anomalies (MCA). This technique can detect small copy number variations (CNVs) in DNA and help to understand the genetic causes in newborns. MATERIALS & METHODS: The present study investigated a group of 63 newborns with MCA during the study period. Microarray analysis was performed on newborns with MCA...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 40650423
DOI: 10.1002/bdr2.2509

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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