Associated Papers
Whole exome sequencing identifies a novel homozygous missense mutation of LHCGR gene in primary infertile women with empty follicle syndrome.
Xu Y et al.
The Journal of Obstetrics and Gynaecology Research, 2023
Novel mutations in LHCGR (luteinizing hormone/choriogonadotropin receptor): expanding the spectrum of mutations responsible for human empty follicle syndrome.
Zhang Z et al.
Journal of Assisted Reproduction and Genetics, 2020
Pregnancy and Live Birth In Women With Pathogenic LHCGR Variants Using Their Own Oocytes.
Lu X et al.
The Journal of Clinical Endocrinology and Metabolism, 2019
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