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• Balakrishnan, V., Sanghvi, L. D., & Kirk, R. L., Genetic diversity among Australian Aborigines, Australian Institute of Aboriginal Studies, Canberra, 1975, http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1013453/. Details
• Banyer, Joanne Lee, 'Molecular Basis of C4 Protein Deficiency in Aboriginal Australians, and a Molecular C4 Allotyping Technique', PhD thesis, Australian National University, 1994. Also available at https://digitalcollections.anu.edu.au/handle/1885/14036. Details
• Barbato, M. P., Agar, N. S., & Kirk, R. L., Thyroid autoantibodies in aborigines, Medical Journal of Australia, vol. 1, 1980, 543-545 pp, http://www.ncbi.nlm.nih.gov/pubmed/7393039. Details
• Barrett, E., Hepatitis--associated antigen in aboriginal groups in Northern Australia., Medical Journal of Australia, vol. 2, 1972, 472-474 pp, http://www.ncbi.nlm.nih.gov/pubmed/4628420. Details
• Berndt, R.M., Berndt, C.H., 'The Genetic Picture', in The World of the First Australians: An introduction to the traditional life of the Australian Aborigines, pp. 447-455. Details
• Best, J.C., Welch, J.S., Filippich, C., McPhee, L., Treatment of Intestinal Parasites in Australian Aboriginal Children, Medical Journal of Australia, 1976, 14-20 pp, http://www.ncbi.nlm.nih.gov/pubmed/1263912. Details
• Betty, D. J., Chin-Atkins, A. N., Croft, L., Sraml, M., & Easteal, S., Multiple independent origins of the COII/tRNA(Lys) intergenic 9-bp mtDNA deletion in aboriginal Australians, American Journal of Human Genetics, vol. 58, 1996, 428-433 pp, http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1914551/. Details
• Bhatia, K. K., Factors affecting electromorph mutation rates in man: an analysis of data from Australian Aborigines, Annals of Human Biology, vol. 7, 1980, 45-54 pp, http://doi.org/10.1080/03014468000004041. Details
• Bhatia, K. K., Rare allele heterozygosity and relative electromorph mutation rates in man, Annals of Human Biology, vol. 8, 1981, 263-276 pp, http://doi.org/10.1080/03014468100005031. Details
• Bhatia, K. K., Blake, N. M., & Kirk, R. L., The frequency of private electrophoretic variants in Australian aborigines and indirect estimates of mutation rate, Americal Journal of Human Genetics, vol. 31, 1979, 731-740 pp, http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1686050/. Details
• Bhatia, K., Easteal, S., Kirk, R.L, 'A Study of Genetic Distance and the Austronesian/ Non-Austronesian Dichotomy', pp. 195-205. Also available at http://press.anu.edu.au/wp-content/uploads/2011/05/ch1027.pdf. Details
• Bhatia, Kuldeep Kumar, 'The Indirect Estimation of Mutation Rates in Man', PhD thesis, Australian National University, 1981. Details
• Birdsell J.B., Simmons R.T., Graydon J.J., 'Microdifferentiation in blood group gene frequencies among 28 adjacent Aboriginal tribal isolates.', Occasional Papers in Human Biology, Australian Institute of Aboriginal Studies, vol. 2. Details
• Blake, N. M., Glutamic pyruvic transaminase and esterase D types in the Asian-Pacific area, Human Genetics, vol. 35, 1976, 91-102 pp, http://doi.org/10.1007/BF00295623. Details
• Blake, N. M., Genetic variants of carbonic anhydrase in the Asian-Pacific area, Annals of Human Biology, vol. 5, 1978, 557-568 pp, http://doi.org/10.1080/03014467800003241. Details
• Blake, N. M., Genetic variation of red cell enzyme systems in Australian Aboriginal populations, Occasional Papers in Human Biology, Australian Institute of Aboriginal Studies, vol. 2, 1979, 39-82 pp, http://trove.nla.gov.au/work/27873079?selectedversion=NBD2593629&q&versionId=33652959. Details
• Blake, N. M., Placental enzymes: A population genetic study, Acta Anthropologenetica, vol. 8, 1984, 199-207 pp, http://www.ncbi.nlm.nih.gov/pubmed/6152771. Details
• Blake, N. M., & Hayes, C., A population genetic study of phosphoglycolate phosphatase, Annals of Human Biology, vol. 7, 1980, 481-484 pp, http://doi.org/10.1080/03014468000004591. Details
• Blake, N. M., & Kirk, R. L., New genetic variant of 6-phosphogluconate dehydrogenase in Australian Aborigines, Nature, vol. 221, 1969, 278 pp, http://doi.org/10.1038/221278a0. Details
• Blake, N. M., & Kirk, R. L., Widespread distribution of variant forms of carbonic anhydrase in Australian aboriginals, Medical Journal of Australia, vol. 1, 1978, 183-185 pp, http://hdl.handle.net/1885/12702. Details
• Blake, N. M., & Omoto, K., Phosphoglucomutase types in the Asian-Pacific area: a critical review including new phenotypes, Annals of Human Genetics, vol. 38, 1975, 251-273 pp, http://doi.org/10.1111/j.1469-1809.1975.tb00610.x. Details
• Blake, N. M., & Spargo, R. M., Population genetic studies in the Kimberley of Western Australia, Human Heredity, vol. 36, 1986, 286-298 pp, http://doi.org/10.1159/000153645. Details
• Blake, N. M., Kirk, R. L., Lewis, W. H., & Harris, H., Some further peptidase B phenotypes, Annals of Human Genetics, vol. 33, 1970, 301-305 pp, http://doi.org/10.1111/j.1469-1809.1970.tb01654.x. Details
• Blake, N. M., Saha, N., McDermid, E. M., Kirk, R. L., & Crane, G. G., Additional electrophoretic variants of 6-phosphogluconate dehydrogenase, Humangenetik, vol. 21, 1974, 347-354 pp, http://link.springer.com/article/10.1007%2FBF00273373. Details
• Blake, N.M., Kirk, R.L., McDermid, E.M, The Distribution of Blood, Serum Proteins and Enzyme Groups in a Series of Lebanese in Australia, The Australian Journal of Experimental Biology and Medical Science, vol. 51, 1973, 209-220 pp, http://www.ncbi.nlm.nih.gov/pubmed/4197731. Details
• Blumberg, B., Australia antigen and the biology of hepatitis B., Science (New York, N.Y.), vol. 197, 1977, 17-25 pp, http://www.sciencemag.org/content/197/4298/17.full.pdf?sid=555a173f-dc1a-4249-ac61-c224a74c9cf2. Details
• Blumberg, B.S; Sutnick, A.I; London, W.T and Millamn, I., 'Chapter 13: Australia Antigen', in The Liver, The Williams and Wilkins Company, 1972. Details
• Board, P. G., Genetic polymorphism of human erythrocyte glyoxalase II, American Journal of Human Genetics, vol. 32, 1980, 690-694 pp, http://www.ncbi.nlm.nih.gov/pubmed/7424909. Details
• Board, P. G., Further electrophoretic studies of erythrocyte glutathione peroxidase, American Journal of Human Genetics, vol. 35, 1983, 914-918 pp, http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1685840/. Details
• Board, P. G., & Coggan, M., Polymorphism of the A subunit of coagulation factor XIII in the Pacific region. Description of new phenotypes., Human genetics, vol. 59, 1981, 135-136 pp, http://doi.org/10.1007/BF00293062. Details
• Board, P. G., & Coggan, M., Genetic heterogeneity of S-formylglutathione hydrolase, Annals of Human Genetics, vol. 50, 1986, 35-39 pp, http://doi.org/10.1111/j.1469-1809.1986.tb01936.x. Details
• Board, P. G., Coggan, M., & Pidcock, M. E., Genetic heterogeneity of prothrombin (FII), Annals of Human Genetics, vol. 46, 1982, 1-9 pp, http://doi.org/10.1111/j.1469-1809.1982.tb00689.x. Details