Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

Phyllis W. Speiser, Perrin C. White

Research output: Contribution to journalArticle

22 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)411-417
Number of pages7
JournalClinical Endocrinology
Volume49
Issue number4
DOIs
StatePublished - 1998

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Steroid 21-Hydroxylase
Congenital Adrenal Hyperplasia
Gene Deletion
Prenatal Diagnosis
Adrenal Cortex Hormones
Genotype
Newborn Infant
Hormones
Phenotype
Pregnancy
Mutation
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency

ASJC Scopus subject areas

  • Endocrinology

Cite this

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency. / Speiser, Phyllis W.; White, Perrin C.

In: Clinical Endocrinology, Vol. 49, No. 4, 1998, p. 411-417.

Research output: Contribution to journalArticle

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