Steroid disorders in children: Congenital adrenal hyperplasia and apparent mineralocorticoid excess

Proceedings of the National Academy of Sciences of the United States of America

Volumn 96, Issue 22, 1999, Pages 12790-12797

  New, Maria I ^a   Wilson, Robert C ^a  

^a WEILL CORNELL MEDICAL COLLEGE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DEXAMETHASONE; STEROID 21 MONOOXYGENASE;

ARTICLE; CLINICAL FEATURE; CLINICAL PROTOCOL; CONGENITAL ADRENAL HYPERPLASIA; CONSANGUINITY; GENETIC ASSOCIATION; HUMAN; HYPERALDOSTERONISM; HYPERTENSION; PATHOGENESIS; PEDIGREE ANALYSIS; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SEX DIFFERENTIATION; STEROID 21 MONOOXYGENASE DEFICIENCY; STEROIDOGENESIS; VIRILIZATION;

ADRENAL HYPERPLASIA, CONGENITAL; CYTOCHROME P-450 ENZYME SYSTEM; DEXAMETHASONE; FEMALE; GENOTYPE; HUMANS; INFANT, NEWBORN; MALE; MINERALOCORTICOIDS; MUTATION; NEONATAL SCREENING; PEDIGREE; PHENOTYPE; PRENATAL DIAGNOSIS; STEROID 21-HYDROXYLASE;

EID: 0033607164     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.96.22.12790     Document Type: Article

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