A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

作者：Ethylin Wang Jabs, Ulrich Müller, Xiang Li, Liang Ma, Wen Luo, Ian S. Haworth, Ivana J. Klisak, Robert S. Sparkes, Matthew L. Warman, John Butler Mulliken, Malcolm L. Snead, Rob Maxson · 发表于：Cell · 年份：1993 · DOI：10.1016/0092-8674(93)90379-5 · 被引用次数：684 · 研究领域：Craniofacial Disorders and Treatments、Hedgehog Signaling Pathway Studies、Developmental Biology and Gene Regulation