@article{b40a5b21b34341a4911cd7ecf237202c,
title = "Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay",
keywords = "9q22, Basal cell carcinoma syndrome, Basal cell nevus syndrome, Chromosomal deletion, Gorlin syndrome, Metopic craniosynostosis, PTCH1",
author = "Muller, \{Eric A.\} and Swaroop Aradhya and Atkin, \{Joan F.\} and Carmany, \{Erin P.\} and Elliott, \{Alison M.\} and Chudley, \{Albert E.\} and Clark, \{Robin D.\} and Everman, \{David B.\} and Shannon Garner and Hall, \{Bryan D.\} and Herman, \{Gail E.\} and Emma Kivuva and Subhadra Ramanathan and Stevenson, \{David A.\} and Stockton, \{David W.\} and Louanne Hudgins",
note = "Copyright {\textcopyright} 2011 Wiley Periodicals, Inc.",
year = "2012",
month = feb,
doi = "10.1002/ajmg.a.34216",
language = "English",
volume = "158 A",
pages = "391--399",
journal = "American Journal of Medical Genetics, Part A",
issn = "1552-4825",
number = "2",
}