New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidismEduardo Fernández‐Rebollo, Guiomar Pérez de Nanclares, Ana Bernal‐Chico et al.|European Journal of Endocrinology|2010Cited by 107
Coexistence of two different pseudohypoparathyroidism subtypes (Ia and Ib) in the same kindred with independent Gsα coding mutations and <i>GNAS</i> imprinting defectsBeatriz Lecumberri, Murat Bastepe, Eduardo Fernández‐Rebollo et al.|Journal of Medical Genetics|2009Cited by 38