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	1.	Hypophosphatemic rickets and breast milk. [electronic resource] by Reade, T M Scriver, C R Producer: 19790728 In: The New England journal of medicine vol. 300 Availability: No items available. Save to lists Add to cart (remove)
	2.	Renal hypophosphataemia has several mendelian forms. [electronic resource] by Scriver, C R Reade, T M Producer: 19871117 In: Lancet (London, England) vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Management of hereditary metabolic disease. The role of allied health personnel. [electronic resource] by Clow, C L Reade, T M Scriver, C R Producer: 19710706 In: The New England journal of medicine vol. 284 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Outcome of early and long-term management of classical maple syrup urine disease. [electronic resource] by Clow, C L Reade, T M Scriver, C R Producer: 19820313 In: Pediatrics vol. 68 Availability: No items available. Save to lists Add to cart (remove)
	5.	Audiometric evidence for two forms of X-linked hypophosphatemia in humans, apparent counterparts of Hyp and Gy mutations in mouse. [electronic resource] by Boneh, A Reade, T M Scriver, C R Rishikof, E Producer: 19880128 In: American journal of medical genetics vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Oral findings in patients with autosomal dominant hypophosphatemic bone disease and X-linked hypophosphatemia: further evidence that they are different diseases. [electronic resource] by Schwartz, S Scriver, C R Reade, T M Shields, E D Producer: 19881123 In: Oral surgery, oral medicine, and oral pathology vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Serum 1,25-dihydroxyvitamin D levels in normal subjects and in patients with hereditary rickets or bone disease. [electronic resource] by Scriver, C R Reade, T M DeLuca, H F Hamstra, A J Producer: 19781202 In: The New England journal of medicine vol. 299 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Use of phosphate and vitamin D to prevent dwarfism and rickets in X-linked hypophosphatemia. [electronic resource] by Glorieux, F H Scriver, C R Reade, T M Goldman, H Roseborough, A Producer: 19720922 In: The New England journal of medicine vol. 287 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Nephrocalcinosis and its relationship to treatment of hereditary rickets. [electronic resource] by Goodyer, P R Kronick, J B Jequier, S Reade, T M Scriver, C R Producer: 19871214 In: The Journal of pediatrics vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Serum osteocalcin in the treatment of inherited rickets with 1,25-dihydroxyvitamin D3. [electronic resource] by Gundberg, C M Cole, D E Lian, J B Reade, T M Gallop, P M Producer: 19830527 In: The Journal of clinical endocrinology and metabolism vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Ontogeny modifies manifestations of cystinuria genes: implications for counseling. [electronic resource] by Scriver, C R Clow, C L Reade, T M Goodyer, P Auray-Blais, C Giguère, R Lemieux, B Producer: 19850412 In: The Journal of pediatrics vol. 106 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Panostotic fibrous dysplasia: a congenital disorder of bone with unusual facial appearance, bone fragility, hyperphosphatasemia, and hypophosphatemia. [electronic resource] by Cole, D E Fraser, F C Glorieux, F H Jequier, S Marie, P J Reade, T M Scriver, C R Producer: 19830617 In: American journal of medical genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	The Hartnup phenotype: Mendelian transport disorder, multifactorial disease. [electronic resource] by Scriver, C R Mahon, B Levy, H L Clow, C L Reade, T M Kronick, J Lemieux, B Laberge, C Producer: 19870619 In: American journal of human genetics vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	14.	Response to crystalline 1alpha-hydroxyvitamin D3 in vitamin D dependency. [electronic resource] by Reade, T M Scriver, C R Glorieux, F H Nogrady, B Delvin, E Poirier, R Holick, F DeLuca, H F Producer: 19751205 In: Pediatric research vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	X-linked hypophosphatemia: effect of calcitriol on renal handling of phosphate, serum phosphate, and bone mineralization. [electronic resource] by Costa, T Marie, P J Scriver, C R Cole, D E Reade, T M Nogrady, B Glorieux, F H Delvin, E E Producer: 19810424 In: The Journal of clinical endocrinology and metabolism vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)