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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.
Analysis of transforming growth factor beta 1 (TGF-beta1) gene polymorphisms in Turkish patients with scleroderma.
Büyük U, Ates O, Dalyan L, Müsellim B, Ongen G, Topal-Sarikaya A.
Büyük U, et al.
Cell Biochem Funct. 2010 Jun;28(4):274-7. doi: 10.1002/cbf.1649.
Cell Biochem Funct. 2010.
PMID: 20517890
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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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Pathogenic missense variation in PABPC1L/EPAB causes female infertility due to oocyte maturation arrest at the germinal vesicle stage.
Okutman O, Gürbüz AS, Büyük U, Real E, Leconte R, Chennen K, Mayer C, Muller J, Le May N, Viville S.
Okutman O, et al. Among authors: buyuk u.
J Assist Reprod Genet. 2024 Feb;41(2):311-322. doi: 10.1007/s10815-023-03009-1. Epub 2024 Jan 5.
J Assist Reprod Genet. 2024.
PMID: 38177974
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