Author:
White Kenneth E.,Evans Wayne E.,O'Riordan Jeffery L.H.,Speer Marcy C.,Econs Michael J.,Lorenz-Depiereux Bettina,Grabowski Monika,Meitinger Thomas,Strom Tim M.
Publisher
Springer Science and Business Media LLC
Reference24 articles.
1. Winters, R.W., Graham, J.B., Williams, T.F., McFalls, V.W. & Burnett, C.H. A genetic study of familial hypophosphatemia and vitamin D-resistant rickets with a review of the literature. Medicine 37, 97– 142 (1958).
2. Scriver, C.R., MacDonald, W., Reade, T., Glorieux, R.H. & Nogrady, B. Hypophosphatemic nonrachitic bone disease: an entity distinct from X- linked hypophosphatemia in the renal defect, bone involvement, and inheritance. Am. J. Med. Genet. 1, 101–117 (1977).
3. Tieder, M. et al. Hereditary hypophosphatemic rickets with hypercalciuria. N. Engl. J. Med. 312, 611–617 (1985).
4. Econs, M.J. & McEnery, P.T. Autosomal dominant hypophosphatemic rickets/osteomalacia: clinical characterization of a novel renal phosphate-wasting disorder. J. Clin. Endocrinol. Metab. 82, 674–681 (1997).
5. Bianchine, J.W., Stambler, A.A. & Harrison, H.E. Familial hypophosphatemic rickets showing autosomal dominant inheritance. Birth Defects Orig. Artic Ser. 7, 287–295 ( 1971).
Cited by
1364 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献