Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline

June 5, 2017 | Autor: Phyllis Speiser | Categoría: Algorithms, Evidence Based Practice, Comorbidity, Pregnancy, Humans, Mutation, Female, Hormones, Male, Phenotype, Clinical Sciences, Newborn Infant, Genotype, Prenatal Diagnosis, Clinical Endocrinology, Mutation, Female, Hormones, Male, Phenotype, Clinical Sciences, Newborn Infant, Genotype, Prenatal Diagnosis, Clinical Endocrinology

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