Publications by authors named "Matthew Fawkner"

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Idiopathic hyperphosphatasia and TNFRSF11B mutations: relationships between phenotype and genotype.
Belinda Chong, Madhuri Hegde, Matthew Fawkner, Scott Simonet, Hamilton Cassinelli

J Bone Miner Res· December 2003

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A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype.
Tim Cundy, Madhuri Hegde, Dorit Naot, Belinda Chong, Alan King, Matthew Fawkner

Hum Mol Genet· September 2002

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