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Proceedings of the National Academy of Sciences of the United States of America|October 15, 1992
Different missense mutations at the tissue-nonspecific alkaline phosphatase gene locus in autosomal recessively inherited forms of mild and severe hypophosphatasiaP S Henthorn, M Raducha, K N Fedde, et al.
The Journal of Clinical Investigation|July 1, 1990
Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studiesR V Thakker, K E Davies, M P Whyte, et al.
Arthritis and Rheumatism|April 1, 1978
Idiopathic multicentric osteolysis. Report of an affected father and sonM P Whyte, W A Murphy, M Kleerekoper, et al.
The Journal of Clinical Endocrinology and Metabolism|August 15, 2001
X-linked hypophosphatemia attributable to pseudoexons of the PHEX geneP T Christie, B Harding, M A Nesbit, et al.
American Journal of Human Genetics|January 23, 1999
Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13S E Lloyd, A A Pannett, P H Dixon, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|January 1, 1994
Mucopolysaccharidosis VII: postmortem biochemical and pathological findings in a young adult with beta-glucuronidase deficiencyC Vogler, B Levy, J W Kyle, et al.
The American Journal of Medicine|February 1, 1982
Postmenopausal osteoporosis. A heterogeneous disorder as assessed by histomorphometric analysis of Iliac crest bone from untreated patientsM P Whyte, M A Bergfeld, W A Murphy, et al.
The Journal of Clinical Endocrinology and Metabolism|June 1, 1996
Hypophosphatasia: levels of bone alkaline phosphatase immunoreactivity in serum reflect disease severityM P Whyte, D A Walkenhorst, K N Fedde, et al.
Radiology|May 1, 1989
X-linked hypophosphatemia in adults: prevalence of skeletal radiographic and scintigraphic featuresD C Hardy, W A Murphy, B A Siegel, et al.
American Journal of Medical Genetics|May 1, 1990
Infantile hypophosphatasia: autosomal recessive transmission to two related sibshipsC A Moore, J C Ward, M L Rivas, et al.
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