发表研究结果有使用 ab122301?请让我们知道,以便我们可以引用本数据表中的参考文章。

ab122301 被引用在 1 文献中.

  • Smith JD  et al. Exome sequencing identifies a recurrent de novo ZSWIM6 mutation associated with acromelic frontonasal dysostosis. Am J Hum Genet 95:235-40 (2014). PubMed: 25105228

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"

注册