Molecular biology of hypophosphataemic rickets and oncogenic osteomalacia
- 1 November 1994
- journal article
- review article
- Published by Springer Nature in Human Genetics
- Vol. 94 (5) , 457-467
- https://doi.org/10.1007/bf00211008
Abstract
No abstract availableKeywords
This publication has 80 references indexed in Scilit:
- Use of Alu-PCR to characterize hybrids containing multiple fragments and to generate new Xp21.3–p22.2 markersGenomics, 1992
- Bridging markers defining the map position of X linked hypophosphataemic rickets.Journal of Medical Genetics, 1987
- Defective adaptation to a low phosphate environment by cultured renal tubular cells from X-linked hypophosphatemic (Hyp) miceBiochemical and Biophysical Research Communications, 1987
- Hypophosphatemic rickets/osteomalacia in linear sebaceous nevus syndrome: A variant of tumor-induced osteomalaciaThe Journal of Pediatrics, 1986
- Bone Response to Phosphate Salts, Ergocalciferol, and Calcitriol in Hypophosphatemic Vitamin D-Resistant RicketsNew England Journal of Medicine, 1980
- Evidence for an Intrinsic Renal Tubular Defect in Mice with Genetic Hypophosphatemic RicketsJournal of Clinical Investigation, 1979
- Serum 1,25-Dihydroxyvitamin D Levels in Normal Subjects and in Patients with Hereditary Rickets or Bone DiseaseNew England Journal of Medicine, 1978
- Basic and Clinical Concepts Related to Vitamin D Metabolism and ActionNew England Journal of Medicine, 1977
- Vitamin D-resistant rickets associated withepidermal nevus syndrome: Demonstration of a phosphaturic substance in the dermal lesionsThe Journal of Pediatrics, 1977
- New method for mapping genes in human chromosomesNature, 1975