Duplication of 18q21.32-q22.3 identified in a stillborn and two relatives with minimal dysmorphic features

Am J Med Genet A. 2012 Jul;158A(7):1788-92. doi: 10.1002/ajmg.a.35405. Epub 2012 May 31.

Authors

Kaylee E Henson¹, Karrie A Hines, David D Weaver, Wilfredo M Torres, Jennifer Verbrugge, Kristyne Stone, Gail H Vance

Affiliation

¹ Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana 46256, USA. khenson@ecommunity.com

PMID: 22653737
DOI: 10.1002/ajmg.a.35405

No abstract available

Publication types

Case Reports

MeSH terms

Abnormalities, Multiple / diagnosis
Abnormalities, Multiple / genetics*
Child, Preschool
Chromosomes, Human, Pair 18
Family
Female
Genetic Association Studies
Humans
Phenotype
Stillbirth
Trisomy*
Young Adult

Supplementary concepts

Chromosome 18, trisomy 18q