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Phenotypic heterogeneity associated with the splicing mutation in congenital adrenal hyperplasia due to 21-hydroxylase deficiency [1]

  • W. L. Miller
  • , S. F. Witchel
  • , D. Bhamidipati
  • , E. P. Hoffman
  • , J. B. Cohen

Research output: Contribution to journalLetterpeer-review

4 Scopus citations
Original languageEnglish
Pages (from-to)1304
Number of pages1
JournalJournal of Clinical Endocrinology and Metabolism
Volume82
Issue number4
DOIs
StatePublished - 1997

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