Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure Article

Qin, Yingying, Jiao, Xue, Dalgleish, Raymond et al. (2014). Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure . FERTILITY AND STERILITY, 101(4), 1104-U548. 10.1016/j.fertnstert.2014.01.001

Open Access International Collaboration

cited authors

  • Qin, Yingying; Jiao, Xue; Dalgleish, Raymond; Vujovic, Svetlana; Li, Jin; Simpson, Joe Leigh; Al-Azzawi, Farook; Chen, Zi-Jiang

publication date

  • April 1, 2014

published in

keywords

  • ALPHA
  • EXPRESSION
  • INSUFFICIENCY
  • LHX8
  • Life Sciences & Biomedicine
  • MUTATION
  • NOBOX
  • Obstetrics & Gynecology
  • Premature ovarian failure (POF)
  • Reproductive Biology
  • SOHLH2
  • Science & Technology
  • TRANSCRIPTION FACTOR
  • WOMEN
  • ovarian function
  • primary ovarian insufficiency (POI)
  • variation

Digital Object Identifier (DOI)

publisher

  • ELSEVIER SCIENCE INC

start page

  • 1104

end page

  • U548

volume

  • 101

issue

  • 4