Medical genetics: advances in brief: A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
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N S Thakker. "Medical genetics: advances in brief: A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis." Journal of Medical Genetics 31.2 (1994) 176-176