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Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect.
Genes (Basel). 2020 Apr 1;11(4):382. doi: 10.3390/genes11040382.
Genes (Basel). 2020.
PMID: 32244758
Free PMC article.
A novel method of multiplex SNP genotyping assay through variable fragment length allele-specific polymerase chain reaction: Multiplex VFLASP-ARMS.
Ünsal SG, Yeni O, Büyük U, Özden Çiftçi Y.
Ünsal SG, et al. Among authors: buyuk u.
Mol Cell Probes. 2024 Apr 8;75:101960. doi: 10.1016/j.mcp.2024.101960. Online ahead of print.
Mol Cell Probes. 2024.
PMID: 38583643
Free article.
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