Editorial: Molecular and Cytogenetic Research Advances in Human Reproduction
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Editorial: Molecular and cytogenetic research advances in human reproduction - volume II.
Chu X, Bukhari I, Thorne R, Shi Q Front Endocrinol (Lausanne). 2023; 14:1232953.
PMID: 37529612 PMC: 10390250. DOI: 10.3389/fendo.2023.1232953.
References
1.
Liu Y, Zhuang X, An J, Jiang H, Li R, Qiao J
. Identification of risk genes in Chinese nonobstructive azoospermia patients based on whole-exome sequencing. Asian J Androl. 2022; 25(1):66-72.
PMC: 9933954.
DOI: 10.4103/aja202275.
View
2.
Fei C, Zhou L
. Gene mutations impede oocyte maturation, fertilization, and early embryonic development. Bioessays. 2022; 44(10):e2200007.
DOI: 10.1002/bies.202200007.
View
3.
Li Y, Wu Y, Jiang H, Khan R, Han Q, Iqbal F
. The molecular control of meiotic double-strand break (DSB) formation and its significance in human infertility. Asian J Androl. 2021; 23(6):555-561.
PMC: 8577252.
DOI: 10.4103/aja.aja_5_21.
View
4.
Wu C, Wang L, Iqbal F, Jiang X, Bukhari I, Guo T
. Preferential Y-Y pairing and synapsis and abnormal meiotic recombination in a 47,XYY man with non obstructive azoospermia. Mol Cytogenet. 2016; 9:9.
PMC: 4736128.
DOI: 10.1186/s13039-016-0218-z.
View
5.
Fan S, Jiao Y, Khan R, Jiang X, Javed A, Ali A
. Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans. Am J Hum Genet. 2021; 108(2):324-336.
PMC: 7895996.
DOI: 10.1016/j.ajhg.2021.01.010.
View