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Journal of Dental Research|February 27, 2015
Periodontal Defects in the A116T Knock-in Murine Model of OdontohypophosphatasiaB L Foster, C R Sheen, N E Hatch, et al.European Journal of Human Genetics : EJHG|October 22, 1998
First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4qM Devoto, K Shimoya, J Caminis, et al.The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
Mutational analysis of PHEX gene in X-linked hypophosphatemiaP H Dixon, P T Christie, C Wooding, et al.Medicine|May 1, 1997
Paget bone disease involving young adults in 3 generations of a Korean familyG S Kim, S H Kim, J K Cho, et al.Molecular Genetics and Metabolism|December 26, 2001
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementiaM J Kovach, B Waggoner, S M Leal, et al.The Journal of Clinical Endocrinology and Metabolism|November 26, 2010
Alendronate for the treatment of pediatric osteogenesis imperfecta: a randomized placebo-controlled studyL M Ward, F Rauch, M P Whyte, et al.Pageof 16