Biblio

Author Title Type [ Year(Asc)]
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2019
Xiao, N., He, K., Gong, F., Xie, Q., Peng, J., Su, X., Lu, Y., Xia, X., Lin, G., and Cheng, L. (2019). Altered subsets and activities of B lymphocytes in polycystic ovary syndrome.J Allergy Clin Immunol.
Wang, H., Meng, L., Li, W., Du, J., Tan, Y., Gong, F., Lu, G., Lin, G., and Zhang, Q. (2019). Combinations of exonic deletions and rare mutations lead to misdiagnosis of propionic acidemia.Clin Chim Acta.
Liu, L., Leng, L., Liu, C., Lu, C., Yuan, Y., Wu, L., Gong, F., Zhang, S., Wei, X., Wang, M., et al. (2019). An integrated chromatin accessibility and transcriptome landscape of human pre-implantation embryos.Nat Commun10, 364.
He, H., Jing, S., Lu, C.Fu, Tan, Y.Qiu, Luo, K.Li, Zhang, S.Ping, Gong, F., Lu, G.Xiu, and Lin, G. (2019). Neonatal outcomes of live births after blastocyst biopsy in preimplantation genetic testing cycles: a follow-up of 1,721 children.Fertil Steril.
Xie, P., Hu, L., Tan, Y., Gong, F., Zhang, S., Xiong, B., Peng, Y., Lu, G.Xiu, and Lin, G. (2019). Retrospective analysis of meiotic segregation pattern and interchromosomal effects in blastocysts from inversion preimplantation genetic testing cycles.Fertil Steril.
Dai, C., Chen, Y., Hu, L., Du, J., Gong, F., Dai, J., Zhang, S., Wang, M., Chen, J., Guo, J., et al. (2019). ZP1 mutations are associated with empty follicle syndrome: evidence for the existence of an intact oocyte and a zona pellucida in follicles up to the early antral stage. A case report.Hum Reprod.