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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 1, 1996
Juvenile Paget disease: life-long features of a mildly affected young womanD S Golob, W H McAlister, B G Mills, et al.The Journal of Clinical Investigation|April 1, 1995
Alkaline phosphatase: placental and tissue-nonspecific isoenzymes hydrolyze phosphoethanolamine, inorganic pyrophosphate, and pyridoxal 5'-phosphate. Substrate accumulation in carriers of hypophosphatasia corrects during pregnancyM P Whyte, M Landt, L M Ryan, et al.Journal of Dental Research|January 8, 2011
Enzyme replacement therapy prevents dental defects in a model of hypophosphatasiaM D McKee, Y Nakano, D L Masica, et al.Journal of the American Veterinary Medical Association|October 1, 1994
Periarticular hyperostosis and renal disease in six black lemurs of two family groupsR E Junge, K G Mehren, T P Meehan, et al.The Journal of Clinical Endocrinology and Metabolism|May 1, 1995
Pseudohypoparathyroidism type Ib is not caused by mutations in the coding exons of the human parathyroid hormone (PTH)/PTH-related peptide receptor geneE Schipani, L S Weinstein, C Bergwitz, et al.Human Genetics|July 1, 1993
New markers for linkage analysis of X-linked hypophosphataemic ricketsP S Rowe, J Goulding, A Read, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 29, 2000
Expansile skeletal hyperphosphatasia: a new familial metabolic bone diseaseM P Whyte, B G Mills, W R Reinus, et al.The American Journal of Medicine|September 1, 1992
Significant developmental elevation in serum parathyroid hormone levels in a large kindred with familial benign (hypocalciuric) hypercalcemiaC T McMurtry, F W Schranck, D A Walkenhorst, et al.Human Genetics|January 1, 1996
Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1D Trump, G Pilia, P H Dixon, et al.Journal of Medical Genetics|December 1, 1987
Bridging markers defining the map position of X linked hypophosphataemic ricketsR V Thakker, A P Read, K E Davies, et al.Pageof 16