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A new heterozygous mutation of the FOXL2 gene is associated with a large ovarian cyst and ovarian dysfunction in an adolescent girl with blepharophimosis/ptosis/epicanthus inversus syndrome

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اقرأ أكثر حفظ في قائمتي
  • معلومة اضافية
    • الموضوع:
      2005
    • Collection:
      Ruhr-Universität Bochum (RUB): Campus Research Bibliography
    • File Description:
      353–358
    • ISSN:
      0804-4643
    • Relation:
      urn:issn:0804-4643
    • الرقم المعرف:
      edsbas.57A07A0A