Chromosome 16p13.11 Microdeletion Syndrome in a Newborn: A Case Study.

We present a case report of an infant diagnosed with chromosome 16p13.11 microdeletion. A discussion of genetic influences, associated clinical manifestations, diagnostics, management, and health promotion strategies are presented to establish core knowledge of chromosome 16p13.11 microdeletion. PMID: 30567812 [PubMed - in process]

https://www.ncbi.nlm.nih.gov/pubmed/30567812?dopt=Abstract

Source: Neonatal Network - September 1, 2018 Category: Perinatology & Neonatology Authors: Smith AE, Jnah A, Newberry D Tags: Neonatal Netw Source Type: research