摘要
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.
基金
supported by the Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences(2020PT320-003,2021-PT320-001)
the National Natural Science Foundation of China(81830043)。
