Bibliography

Angastiniotis M and Modell B, 1998. Global Epidemiology of Hemoglobin Disorders. Annals of the New York Academy of Sciences, 850: 251-269.

Barlow-Stewart K, 2004. Thalassaemia. In The Australasian Genetics Resource Book (Ed Barlow-Stewart K), Centre for Genetics Education, Royal North Shore Hospital, Sydney NSW

NSW ISBN 0-9580797-2-2.
http://www.genetics.com.au

Bowden DK, 2001. Screening for thalassaemia. Australian Prescriber, 24: 120.

Gaff C, Newstead J and Metcalfe S, 2003. Thalassaemia disorders. In The Genetics File. Victorian
Department of Human Services, Melbourne. ISBN 0 7311 61777.
http://www.mcri.edu.au/GF/pages/GeneticsFile.asp

Petrou V, Bowden D, 2005. Suggested protocol for targeted testing of high risk populations.
Medical Therapy Unit, Monash Medical Centre, Victoria, Australia (adapted).

World Health Organization, accessed December 9, 2005.
http://www.who.int/genomics/public/Maphaemoglobin.pdf

Yenchitsomanus PT, Summers KM, Bhattia, Board PG, 1986. A single alpha-globin gene deletion in Australian aborigines. Australian Journal of Experimental Biology and Medical Science, 64: 297-306.

Tsintsof AS, Hertzberg MS, Prior JF, Mickelson KN, Trent RJ, 1990. Alpha-globin gene markers identify genetic differences between Australian aborigines and Melanesians. American Journal of Human Genetics, 46: 138-143.

Prior JF, Bennett JA, Erber WN, 2004. The incidence of α-thalassaemia in an Indigenous Australian community. Genetics and Population Health, Fremantle, P5.