Nonsense mutation of EMX2 is potential causative for uterus didelphysis: first molecular explanation for isolated incomplete mullerian fusion Article

Liu, Shan, Gao, Xuan, Qin, Yingying et al. (2015). Nonsense mutation of EMX2 is potential causative for uterus didelphysis: first molecular explanation for isolated incomplete mullerian fusion . 103(3), 769-U489. 10.1016/j.fertnstert.2014.11.030

International Collaboration

cited authors

  • Liu, Shan; Gao, Xuan; Qin, Yingying; Liu, Wen; Huang, Tao; Ma, Jinlong; Simpson, Joe Leigh; Chen, Zi-Jiang

fiu authors

publication date

  • March 1, 2015

keywords

  • 192 CHINESE WOMEN
  • DUCT ABNORMALITIES
  • Dominant negative effect
  • EMX2
  • FEMALE REPRODUCTIVE-TRACT
  • GENETICS
  • LHX1
  • Life Sciences & Biomedicine
  • Obstetrics & Gynecology
  • P63
  • Reproductive Biology
  • Science & Technology
  • WNT5A
  • incomplete mullerian fusion
  • mullerian duct anomalies

Digital Object Identifier (DOI)

start page

  • 769

end page

  • U489

volume

  • 103

issue

  • 3