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H.H. Dahl

Gene Identification and Expression Laboratory

Murdoch Childrens Research institute

Parkville

Victoria

Australia

[email]@*.rch.unimelb.edu.au

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Affiliations

Gene Identification and Expression Laboratory, Murdoch Childrens Research institute, Parkville, Victoria, Australia. 2001 - 2003
The Murdoch Institute, Royal Children's Hospital, Melbourne, Australia. 1998 - 2000

References

Language and speech perception outcomes in hearing-impaired children with and without connexin 26 mutations. Dahl, H.H., Wake, M., Sarant, J., Poulakis, Z., Siemering, K., Blamey, P. Audiol. Neurootol. (2003) [Pubmed]
Mitochondrial diseases: beyond the magic circle. Dahl, H.H., Thorburn, D.R. Am. J. Med. Genet. (2001) [Pubmed]
Towards reliable prenatal diagnosis of mtDNA point mutations: studies of nt8993 mutations in oocytes, fetal tissues, children and adults. Dahl, H.H., Thorburn, D.R., White, S.L. Hum. Reprod. (2000) [Pubmed]
Getting to the nucleus of mitochondrial disorders: identification of respiratory chain-enzyme genes causing Leigh syndrome. Dahl, H.H. Am. J. Hum. Genet. (1998) [Pubmed]