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Proceedings of the National Academy of Sciences of the United States of America|October 1, 1988
A missense mutation in the human liver/bone/kidney alkaline phosphatase gene causing a lethal form of hypophosphatasiaM J Weiss, D E Cole, K Ray, et al.Journal of Dental Research|October 26, 2005
Cementum and dentin in hypophosphatasiaT van den Bos, G Handoko, A Niehof, et al.Human Genetics|August 1, 1995
Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBHD Trump, M P Whyte, C Wooding, et al.Journal of Medical Genetics|December 1, 1998
Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27D Trump, P H Dixon, S Mumm, et al.The American Journal of Medicine|July 1, 1980
Osteopetrosis, renal tubular acidosis and basal ganglia calcification in three sistersM P Whyte, W A Murphy, M D Fallon, et al.Molecular Medicine (Cambridge, Mass.)|May 1, 1996
Osteopenia in 37 members of seven families: analysis based on a model of dominant inheritanceL D Spotila, J Caminis, M Devoto, et al.The Journal of Pediatrics|December 1, 1984
Enzyme replacement therapy for infantile hypophosphatasia attempted by intravenous infusions of alkaline phosphatase-rich Paget plasma: results in three additional patientsM P Whyte, W H McAlister, L S Patton, et al.American Journal of Human Genetics|May 1, 1989
Analysis of liver/bone/kidney alkaline phosphatase mRNA, DNA, and enzymatic activity in cultured skin fibroblasts from 14 unrelated patients with severe hypophosphatasiaM J Weiss, K Ray, M D Fallon, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 1, 1997
Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneityJ M Gertner, M P Whyte, P H Dixon, et al.Genomics|April 13, 1999
Transcription map of Xq27: candidates for several X-linked diseasesI Zucchi, J Jones, M Affer, et al.Pageof 16