A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
Open Access
- 1 November 1993
- journal article
- research article
- Published by Elsevier BV in Cell
- Vol. 75 (3), 443-450
- https://doi.org/10.1016/0092-8674(93)90379-5
Abstract
No abstract availableKeywords
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