Clinical implications of genetic defects in G proteins. The molecular basis of McCune-Albright syndrome and Albright hereditary osteodystrophy

• RINGEL MD

収録刊行物

• Medicine (Baltimore)

  Medicine (Baltimore) 75 171-184, 1996

詳細情報

• CRID: 1572543025480886912
• NII論文ID: 10021264933
• データソース種別:
  • CiNii Articles