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Pediatrics|December 1, 1981
Outcome of early and long-term management of classical maple syrup urine diseaseC L Clow, T M Reade, C R ScriverAmerican Journal of Medical Genetics|August 1, 1987
Audiometric evidence for two forms of X-linked hypophosphatemia in humans, apparent counterparts of Hyp and Gy mutations in mouseA Boneh, T M Reade, C R Scriver, et al.Oral Surgery, Oral Medicine, and Oral Pathology|September 1, 1988
Oral findings in patients with autosomal dominant hypophosphatemic bone disease and X-linked hypophosphatemia: further evidence that they are different diseasesS Schwartz, C R Scriver, T M Reade, et al.The New England Journal of Medicine|November 2, 1978
Serum 1,25-dihydroxyvitamin D levels in normal subjects and in patients with hereditary rickets or bone diseaseC R Scriver, T M Reade, H F DeLuca, et al.The Journal of Pediatrics|November 1, 1987
Nephrocalcinosis and its relationship to treatment of hereditary ricketsP R Goodyer, J B Kronick, S Jequier, et al.The Journal of Pediatrics|March 1, 1985
Ontogeny modifies manifestations of cystinuria genes: implications for counselingC R Scriver, C L Clow, T M Reade, et al.Pediatric Research|July 1, 1975
Response to crystalline 1alpha-hydroxyvitamin D3 in vitamin D dependencyT M Reade, C R Scriver, F H Glorieux, et al.American Journal of Human Genetics|May 1, 1987
The Hartnup phenotype: Mendelian transport disorder, multifactorial diseaseC R Scriver, B Mahon, H L Levy, et al.American Journal of Medical Genetics|April 1, 1983
Panostotic fibrous dysplasia: a congenital disorder of bone with unusual facial appearance, bone fragility, hyperphosphatasemia, and hypophosphatemiaD E Cole, F C Fraser, F H Glorieux, et al.Ciba Foundation Symposium|June 27, 1979
On being an individual, or: the man in the red hatC R ScriverPageof 18