No association between polymorphisms in PTEN and primary ovarian insufficiency in a Han Chinese population

Por Zou, Weiwei, Wang, Binbin, Wang, Jing, Zhang, Zhiguo, Xu, Xiaofeng, Chen, Beili, Ma, Xu, Cao, Yunxia
Publicado no Reprod Biol Endocrinol (2015)

A novel mutation of HOXA11 in a patient with septate uterus

Por Zhu, Ying, Cheng, Zhi, Wang, Jing, Liu, Beihong, Cheng, Longfei, Chen, Beili, Cao, Yunxia, Wang, Binbin
Publicado no Orphanet J Rare Dis (2017)

Mutation analysis of the WNT4 gene in Han Chinese women with premature ovarian failure

Por Chen, Beili, Suo, Peisu, Wang, Binbin, Wang, Jing, Yang, Lu, Zhou, Sirui, Zhu, Ying, Ma, Xu, Cao, Yunxia
Publicado em 2011

Consanguineous familial study revealed biallelic FIGLA mutation associated with premature ovarian insufficiency

Por Chen, Beili, Li, Lin, Wang, Jing, Li, Tengyan, Pan, Hong, Liu, Beihong, Zhou, Yiran, Cao, Yunxia, Wang, Binbin
Publicado no J Ovarian Res (2018)

Successful preimplantation genetic diagnosis by targeted next-generation sequencing on an ion torrent personal genome machine platform

Por Hao, Yan, Chen, Dawei, Zhang, Zhiguo, Zhou, Ping, Cao, Yunxia, Wei, Zhaolian, Xu, Xiaofeng, Chen, Beili, Zou, Weiwei, Lv, Mingrong, Ji, Dongmei, He, Xiaojin
Publicado no Oncol Lett (2018)