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Toxicological Sciences : an Official Journal of the Society of Toxicology|June 6, 2006
Phenotypic anchoring of acetaminophen-induced oxidative stress with gene expression profiles in rat liverChristine L Powell, Oksana Kosyk, Pamela K Ross, et al.Bone|March 11, 2015
Osteoblast differentiation profiles define sex specific gene expression patterns in craniosynostosisSarah S Park, Richard P Beyer, Matthew D Smyth, et al.American Journal of Medical Genetics. Part A|August 5, 2010
Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosisHeather C Mefford, Neil Shafer, Francesca Antonacci, et al.American Journal of Human Genetics|August 9, 2014
Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosisJoshua D Smith, Anne V Hing, Christine M Clarke, et al.Human Mutation|July 26, 2012
ALX4 gain-of-function mutations in nonsyndromic craniosynostosisGarima Yagnik, Apar Ghuman, Sundon Kim, et al.Biology of Sex Differences|April 26, 2016
Using the 3D Facial Norms Database to investigate craniofacial sexual dimorphism in healthy children, adolescents, and adultsMatthew J Kesterke, Zachary D Raffensperger, Carrie L Heike, et al.Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|September 9, 2024
Tracheal Ultrasound for Diagnosis of Tracheal Cartilaginous Sleeve in Patients with Syndromic CraniosynostosisClare M Richardson, Austin S Lam, Grace E Nicholas, et al.Journal of Cell Science|December 15, 2015
Activation of the IGF1 pathway mediates changes in cellular contractility and motility in single-suture craniosynostosisZeinab Al-Rekabi, Marsha M Wheeler, Andrea Leonard, et al.The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|October 23, 2015
The 3D Facial Norms Database: Part 1. A Web-Based Craniofacial Anthropometric and Image Repository for the Clinical and Research CommunitySeth M Weinberg, Zachary D Raffensperger, Matthew J Kesterke, et al.Human Genetics|September 27, 2003
Increased risk for developmental delay in Saethre-Chotzen syndrome is associated with TWIST deletions: an improved strategy for TWIST mutation screeningJuanliang Cai, Barbara K Goodman, Ankita S Patel, et al.Pageof 16