3q29 Chromosomal duplication in a neonate with associated myelomeningocele and midline cranial defects

Clin Dysmorphol. 2017 Oct;26(4):221-223. doi: 10.1097/MCD.0000000000000193.

Authors

Marley B Lawrence¹, Alexandra Arreola, Michael Cools, Scott Elton, Karen S Wood

Affiliation

¹ Departments of aPediatrics bPathology and Laboratory Medicine cNeurosurgery dDivision of Neonatal-Perinatal Medicine, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

PMID: 28763312
DOI: 10.1097/MCD.0000000000000193

No abstract available

Publication types

Case Reports

MeSH terms

Chromosome Duplication / genetics*
Chromosomes, Human, Pair 3 / genetics*
Female
Humans
Infant
Infant, Newborn
Magnetic Resonance Imaging
Meningomyelocele / diagnostic imaging
Meningomyelocele / genetics*
Meningomyelocele / pathology
Radiography, Thoracic
Skull / abnormalities*
Skull / diagnostic imaging
Skull / pathology