Genetic basis of endocrine disease 2: Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Perrin C. White, Maria I. New

Research output: Contribution to journalArticle

89 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)6-11
Number of pages6
JournalJournal of Clinical Endocrinology and Metabolism
Volume74
Issue number1
StatePublished - Jan 1992

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Virilism
Steroid 21-Hydroxylase
Endocrine System Diseases
Congenital Adrenal Hyperplasia
Chromosome Deletion
Prenatal Diagnosis
Phenotype
Mutation
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency

ASJC Scopus subject areas

  • Biochemistry
  • Endocrinology, Diabetes and Metabolism

Cite this

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