Cover Image, Volume 173A, Number 10, October 2017

Rani A Bashir; Abhijit Dixit; Caitlin Goedhart; Jillian S Parboosingh; Allan M Innes; Care for Rare Canada Consortium; Patrick Ferreira; Shabih U Hasan; Ping-Yee B Au

doi:10.1002/ajmg.a.38481

Cover Image, Volume 173A, Number 10, October 2017

Am J Med Genet A. 2017 Oct;173(10):i. doi: 10.1002/ajmg.a.38481.

Authors

Affiliations

¹ Department of Pediatrics, Section of Neonatal-Perinatal Medicine, University of Calgary, Calgary, Alberta, Canada.
² Clinical Genetics, City Campus, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
³ Department of Medical Genetics, University of Calgary, Calgary, Alberta, Canada.
⁴ Alberta Children's Hospital Research Institute, University of Calgary, Calgary, Alberta, Canada.

PMID: 28921853
DOI: 10.1002/ajmg.a.38481

Abstract

The cover image, by Rani A. Bashir et al., is based on the Original Article Lin-Gettig syndrome: Craniosynostosis expands the spectrum of the KAT6B related disorders, DOI: 10.1002/ajmg.a.38355.

MeSH terms

Craniosynostoses / genetics
Craniosynostoses / pathology*
Histone Acetyltransferases / genetics*
Humans
Mutation*
Phenotype*
Syndrome

Substances

Histone Acetyltransferases
KAT6B protein, human