Associated Papers
Mutations in CCNB3 affect its location thus causing a multiplicity of phenotypes in human oocytes maturation by aberrant CDK1 activity and APC/C activity at different stages.
Wang C et al.
Journal of Ovarian Research, 2023
Identification of genetic polymorphisms in unexplained recurrent spontaneous abortion based on whole exome sequencing.
Mou JT et al.
Annals of Translational Medicine, 2022
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy.
Fatemi N et al.
Journal of Medical Genetics, 2021
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