Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from Southern Germany

• KRONE N

収録刊行物

• J Clin Endocrinol Metab

  J Clin Endocrinol Metab 85 1059-1065, 2000

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• CRID: 1571417125574486272
• NII論文ID: 10021265523
• データソース種別:
  • CiNii Articles