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craniosynostosis, type 2
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MSX2
[Molecular cloning and expression of homeobox-containing genes during hard tissue development]
Expression of a human homeobox-containing gene is regulated by 1,25(OH)2D3 in bone cells
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
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External
Whole-Heart Myocardial Blood Flow Quantification Using MRI