Mutations in MEOX1, Encoding Mesenchyme Homeobox 1, Cause Klippel-Feil Anomaly
- 3 January 2013
- journal article
- case report
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 92 (1), 157-161
- https://doi.org/10.1016/j.ajhg.2012.11.016
Abstract
No abstract availableKeywords
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