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首页> 外文期刊>Clinical dysmorphology >A new syndromic craniosynostosis with involvement of the spine, long bones, pelvis, and digits: Molecular genetic and array analysis
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A new syndromic craniosynostosis with involvement of the spine, long bones, pelvis, and digits: Molecular genetic and array analysis

机译:涉及脊柱,长骨,骨盆和手指的新型综合征性颅骨融合症:分子遗传学和阵列分析

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摘要

We examined single-nucleotide polymorphisms (SNPs) in IL18 and IL18/R1 genes and knee OA. IL18 rs1946518 wild-type allele was more frequently observed in cases (P=0.04). Haplotype 1 was more frequently observed in cases (P=0.04). Genetic variation in the promoter region of IL18, but not IL18R1, may be associated with OA.
机译:我们检查了IL18和IL18 / R1基因和膝OA中的单核苷酸多态性(SNP)。在病例中,IL18 rs1946518野生型等位基因更为常见(P = 0.04)。在这种情况下,单倍型1更常见(P = 0.04)。 IL18而非IL18R1启动子区域的遗传变异可能与OA有关。

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