Growth hormone deficiency with advanced bone age phenotypic interaction between GHRH receptor and CYP21A2 mutations diagnosed by sanger and whole exome sequencing
Fernanda A. Correa Marcela M França; Qing Fang; Qianyi Ma; Tânia Aparecida Sartori Sanchez Bachega; Andresa Rodrigues; Bilge A Ozel; Jun Z Li; Berenice Bilharinho de Mendonça; Alexander Augusto de Lima Jorge; Luciani R Carvalho; Sally A Camper; Ivo J Arnhold
Archives of endocrinology metabolism v. 61, n. 6, p. 633-636, 2017Rio De Janeiro, Rj 2017
Localização: FM - Fac. Medicina (BCSEP 250 2017 )(Acessar)