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)
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bcsep 251 2010
bcsep 249 2017@3
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