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Arquivos Brasileiros De Endocrinologia E Metabologia|September 12, 2014
3β-hydroxysteroid dehydrogenase type II deficiency on newborn screening testVitor Guilherme Brito de Araújo, Renata Santarem de Oliveira, Kallianna Paula Duarte Gameleira, et al.
Endocrine|September 23, 2018
Insights on the phenotypic heterogenity of 11β-hydroxylase deficiency: clinical and genetic studies in two novel familiesLuciana Pinto Valadares, Alessandra Christine Vieira Pfeilsticker, Selma Moreira de Brito Sousa, et al.
Journal of the Endocrine Society|May 2, 2019
MKRN3 Mutations in Central Precocious Puberty: A Systematic Review and Meta-AnalysisLuciana Pinto Valadares, Cinthia Gabriel Meireles, Isabela Porto De Toledo, et al.
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