Associated Papers
Novel mutations in FSIP2 cause male infertility through multiple morphological abnormalities of the sperm flagella.
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Asian Journal of Andrology, 2025
Novel variants of FSIP2 and SPEF2 cause varying degrees of spermatozoa damage in MMAF patients and favorable ART outcomes.
Dai CL et al.
Journal of Assisted Reproduction and Genetics, 2025
Exome sequencing in fetuses with short long bones detected by ultrasonography: A retrospective cohort study.
Huang Y et al.
Frontiers in Genetics, 2023
36923788 (PubMed )
Supplement: Table3.xlsx › Sheet1
Early Onset of Combined Oxidative Phosphorylation Deficiency in Two Chinese Brothers Caused by a Homozygous (Leu275Phe) Mutation in the C1QBP Gene.
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Frontiers in Pediatrics, 2020
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Supplement: Table_2.XLSX › Result
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