Non-syndromic severe hypodontia caused by a novel frameshift insertion mutation in the homeobox of the MSX1 gene

Mushriq F. Abid, M. A. Simpson, Christos Petridis, M. T. Cobourne, P. T. Sharpe*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)

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Biochemistry, Genetics and Molecular Biology