Article
Interstitial deletions of chromosome 1p: novel 1p31.3p22.2 microdeletion in a newborn with craniosynostosis, coloboma and cleft palate, and review of the genomic and phenotypic profiles.
Italian journal of pediatrics - 4 Mar 2022
Serra Gregorio, Antona Vincenzo, Giuffrè Mario, Piro Ettore, Salerno Sergio, Schierz Ingrid Anne Mandy, Corsello Giovanni
Abstract excerpt
BACKGROUND: Rearrangements of unstable DNA sequences may alter the structural integrity or the copy number of dose-sensitive genes, resulting in copy number variations. They may lead more frequently to deletions, in addition to duplications and/or inversions, which are the underlying pathogenic mechanism of a group of conditions known as genomic disorders (or also contiguous gene syndromes). Interstitial...
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