An unusual phenotype of Frasier syndrome due to IVS9 14C> T mutation in the WT1 gene : predominantly male ambiguous genitalia and absence of gonadal dysgenesis

• MELO KF

収録刊行物

• J Clin Endocrinol Metab

  J Clin Endocrinol Metab 87 2500-2505, 2002

詳細情報

• CRID: 1571980075316518528
• NII論文ID: 10018178113
• データソース種別:
  • CiNii Articles