Adrenal Hyperplasia, CongenitalSteroid 21-Hydroxylase17-alpha-HydroxyprogesteroneAdrenal GlandsPregnanetriolHydroxyprogesteronesFludrocortisoneAdrenal Rest TumorAdrenal Gland DiseasesAdrenocortical HyperfunctionVirilismAdrenal InsufficiencyAdrenal Cortex17-KetosteroidsCortodoxoneAdrenal Gland NeoplasmsAdrenal MedullaPhenylalanine HydroxylaseMineralocorticoidsHirsutismSteroid HydroxylasesSteroid 11-beta-Hydroxylase17-alpha-HydroxypregnenoloneAdrenocorticotropic HormoneAntley-Bixler Syndrome PhenotypeTyrosine 3-MonooxygenaseTryptophan HydroxylaseHydrocortisoneAge Determination by SkeletonCosyntropin46, XY Disorders of Sex DevelopmentNeonatal ScreeningMixed Function OxygenasesProcollagen-Proline DioxygenaseDisorders of Sex DevelopmentGlucocorticoidsAndrostenedioneAdrenal Cortex NeoplasmsGenetic Diseases, X-LinkedDAX-1 Orphan Nuclear ReceptorSexual InfantilismAdrenalectomyPuberty, PrecociousGlycerol KinaseReproductive Physiological PhenomenaAndrogensPHEX Phosphate Regulating Neutral EndopeptidaseInfant, NewbornInfant, PostmatureObstetric Surgical ProceduresPrenatal DiagnosisGenitaliaDexamethasoneCholestanetriol 26-MonooxygenaseAdrenal Cortex HormonesPubertyBenzopyrene HydroxylaseUrogenital Abnormalities4-Hydroxybenzoate-3-MonooxygenaseComplement C4HydroxylationTestosteroneHypophosphatemiaSteroidsHypophosphatemia, FamilialMutation3-Hydroxysteroid DehydrogenasesPseudogenesCatecholaminesHeterozygote DetectionFamilial Hypophosphatemic RicketsBody HeightHormone Replacement TherapyCortisoneCytochrome P-450 Enzyme SystemPhenotypeMolecular Sequence DataHeterozygoteTeaching MaterialsFetal DiseasesHydroxyprolinePheochromocytomaPregnancyBase SequenceDopamine beta-HydroxylaseRadioimmunoassayPhenylketonuriasAdrenocortical AdenomaGenotypeDNA Mutational Analysis