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Expert Opinion on Medical Diagnostics|March 19, 2013
Molecular diagnosis of vertebral segmentation disorders in humansPhilip F Giampietro, Sally L Dunwoodie, Kenro Kusumi, et al.American Journal of Medical Genetics. Part A|October 17, 2006
DLL3 as a candidate gene for vertebral malformationsPhilip F Giampietro, Cathleen L Raggio, Cory Reynolds, et al.Scoliosis|September 25, 2007
Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformationsNader Ghebranious, Cathleen L Raggio, Robert D Blank, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 10, 2008
A missense T (Brachyury) mutation contributes to vertebral malformationsNader Ghebranious, Robert D Blank, Cathleen L Raggio, et al.American Journal of Physiology. Heart and Circulatory Physiology|February 4, 2025
Cardiac health, type I collagen, and aging in the <i>oim/oim</i> mouse model of osteogenesis imperfecta and a cohort of adults with OIBrittany N Lafaver, Li Lee, Chloe E Derocher, et al.Lancet (London, England)|August 10, 2013
Risedronate in children with osteogenesis imperfecta: a randomised, double-blind, placebo-controlled trialNick Bishop, Silvano Adami, S Faisal Ahmed, et al.JBMR Plus|May 28, 2019
A Multicenter Observational Cohort Study to Evaluate the Effects of Bisphosphonate Exposure on Bone Mineral Density and Other Health Outcomes in Osteogenesis ImperfectaJaskaran S Bains, Erin M Carter, Kate P Citron, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 15, 2019
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage modelJiaqi Liu, Nan Wu, , et al.Pageof 4