M. Fawkner

Plagiarism, Cheating and Academic Dishonesty – Have You Been There?

M. Fawkner, Greta Keremidchieva, 2004 .

Hierarchical mutation screening protocol for the BRCA1 gene

A. Shelling, M. Hegde, I. Winship, 2000, Human mutation.

Detection of sequence variations in the adenomatous polyposis coli (APC) gene using denaturing high-performance liquid chromatography.

C. Richards, M. Hegde, L. Su, 2001, Genetic testing.

Use of the newborn screening card to define cause of death in a 12‐year‐old diagnosed with epilepsy

J. Skinner, M. Hegde, B. Chong, 2004, Journal of paediatrics and child health.

Microdeletion in the FMR-1 gene: an apparent null allele using routine clinical PCR amplification

S. Warren, M. Hegde, H. Peters, 2001, Journal of medical genetics.

Compound heterozygosity at the FMR1 gene.

M. Hegde, J. Mcgaughran, D. Love, 2001, Genetic testing.

Idiopathic hyperphosphatasia and TNFRSF11B mutations: relationships between phenotype and genotype.

J. Kanis, M. Hegde, B. Tüysüz, 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Idiopathic Hyperphosphatasia and TNFRSF11B Mutations: Relationships Between Phenotype and Genotype

J. Kanis, M. Hegde, B. Tüysüz, 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype.

I. Reid, M. Hegde, J. Mulley, 2002, Human molecular genetics.

Idiopathic Hyperphosphatasia and TNFRSF11B Mutations: Relationships Between Phenotype and Genotype

J. Kanis, M. Hegde, B. Tüysüz, 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.