Author:
Pereda Arrate, ,Garin Intza,Perez de Nanclares Guiomar
Funder
Instituto de Salud Carlos III
Ministerio de Economía y Competitividad
European Regional Development Fund
Department of Health of the Basque Government
Euskal Herriko Unibertsitatea
I3SNS Program of the Spanish Ministry of Health
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference50 articles.
1. Albright F, Burnett CH, Smith PH, Parson W. Pseudohypoparathyroidsm- an example of “Seabright syndrome”. Endocrinology. 1942;30:922–32.
2. Fitch N, Opitz JM, Herrmann J. Albright’s hereditary osteodystrophy: a review. Am J Med Genet. 1982;11:11–29.
3. Albright F, Forbes AP, Henneman PH. Pseudo-pseudohypoparathyroidism. TransAssoc Am Physicians. 1952;65:337–50.
4. Mantovani G, Linglart A, Garin I, Silve C, Elli FM, de Nanclares GP. Clinical utility gene card for: pseudohypoparathyroidism. Eur J Hum Genet. 2013;21
5. Thiele S, Mantovani G, Barlier A, Boldrin V, Bordogna P, De Sanctis L, et al. From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network. Eur J Endocrinol. 2016;175:P1–17.
Cited by
1 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