Phenotypes of 8q13.2-q13.3 microdeletion: Case report and literature review of an emerging recurrent microdeletion syndrome

Am J Med Genet A. 2016 Mar;170(3):804-8. doi: 10.1002/ajmg.a.37497. Epub 2015 Dec 10.

Authors

Mark J Hamilton¹, Ajoy Sarkar¹, Abhijit Dixit¹, Elizabeth Marder²

Affiliations

¹ Department of Clinical Genetics, Nottingham City Hospital, Nottingham University Hospitals NHS Trust, Nottingham, UK.
² Department of Community Paediatrics, Nottingham Children's Hospital, Nottingham University Hospitals NHS Trust, Nottingham, UK.

PMID: 26663483
DOI: 10.1002/ajmg.a.37497

No abstract available

Publication types

Case Reports
Review

MeSH terms

Abnormalities, Multiple / diagnosis
Abnormalities, Multiple / genetics
Child
Chromosome Deletion*
Chromosome Mapping
Chromosomes, Human, Pair 8*
Facies
Genetic Association Studies*
Humans
Male
Phenotype*