Biblio

Author Title Type [ Year(Desc)]
Filters: Author is Lu, Guang-Xiu  [Clear All Filters]
2014
Xu F, Zhang Y-N, Cheng D-H, Tan K, Zhong C-G, Lu G-X, Lin G, Tan Y-Q. The first patient with a pure 1p36 microtriplication associated with severe clinical phenotypes. Mol Cytogenet. 2014;7(1):64.
2018
Zhou Q-W, Jing S, Xu L, Guo H, Lu C-F, Gong F, Lu G-X, Lin G, Gu Y-F. Clinical and neonatal outcomes of patients of different ages following transfer of thawed cleavage embryos and blastocysts cultured from thawed cleavage-stage embryos. PLoS One. 2018;13(11):e0207340.
Zhang Y-X, Li H-Y, Bin He W-, Tu C, Du J, Li W, Lu G-X, Lin G, Yang Y, Tan Y-Q. XRCC2 mutation causes premature ovarian insufficiency as well as non-obstructive azoospermia in humans. Clin Genet. 2018.
2023
Li Q, Wang Y, Zheng W, Guo J, Zhang S, Gong F, Lu G-X, Lin G, Dai J. Biallelic variants in IQCN cause sperm flagellar assembly defects and male infertility. Hum Reprod. 2023.
Che J-F, Wu H-X, Zeng S-C, Wu Y-R, Dai J, Cheng D-H, Gong F, Lu G-X, Lin G, Dai C. Defects in phospholipase C zeta cause polyspermy and low fertilization after conventional IVF: not just ICSI failure. Asian J Androl. 2023.
Guo J, Bin He W-, Dai L, Tian F, Luo Z, Shen F, Tu M, Zheng Y, Zhao L, Tan C, et al. Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192. HGG Adv. 2023:100256.
2024
Cheng D, Lu C-F, Gong F, Du J, Yuan S, Luo K-L, Tan Y-Q, Lu G-X, Lin G. A case report of a normal fertile woman with 46,XX/46,XY somatic chimerism reveals a critical role for germ cells in sex determination. Hum Reprod. 2024.
Luo C, Chen Z, Meng L, Tan C, He W, Tu C, Du J, Lu G-X, Lin G, Tan Y-Q, et al. A hemizygous loss-of-function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia. Clin Genet. 2024.