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Assessing the morphology and ovarian reserve of the ovaries from Mayer-Rokitansky-Küster-Hauser syndrome patients
作者姓名:Ze Liang  Jiali Duan  Duoduo Zhang  Yan You  Lan Zhu
作者单位:1. Department of Obstetrics and Gynecology,National Clinical Research Center for Obstetric & Gynecologic Diseases,State Key Laboratory of Complex Severe and Rare Diseases,Peking Union Medical College Hospital,Chinese Academy of Medical Sciences & Peking Union Medical College;2. 4+4 Medical Doctor Program,Chinese Academy of Medical Sciences & Peking Union Medical College;3. Department of Pathology,Peking Union Medical College Hospital,Chinese Academy of Medical Sciences & Peking Union Medical College
基金项目:the National Natural Science Foundation of China (81830043);
摘    要:<正>Dear Editor,Mayer-Rokitansky-Küster-Hauser(MRKH) syndrome is a rare congenital disease characterized by the hypoplastic uterus and vagina in women with a normal female karyotype(46, XX) and phenotype. Although some genes and mutations, such as WNT4, have been reported in a small portion of MRKH syndrome patients(Biason-Lauber et al.,

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