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Findlay, I., Chan, F-Y., Forbes, K. and Mitchelson, K. R. (2001) High throughput genetic diagnosis of single and small numbers of cells. Today's Life Science, 13 1: 40-46. 49  
Henderson, T. R., Findlay, I., Matthews, P. L. and Noble, B. A. (2001) Identifying the origin of single corneal cells by DNA fingerprinting - Part II - Application to limbal allografting. Cornea, 20 4: 404-407. doi:10.1097/00003226-200105000-00014 41   14 Cited 18 times in Scopus18 0
Henderson, T. R., Findlay, I., Matthews, P. L. and Noble, B. A. (2001) Identifying the origin of single corneal cells by DNA fingerprinting - Part I - Implications for corneal limbal allografting. Cornea, 20 4: 400-403. doi:10.1097/00003226-200105000-00013 40   13 Cited 17 times in Scopus17 0
Findlay, I., Matthews, P., Biros, I., Mitchelson, K., Chan, F-Y. and Forbes, K. L. (2000). Low cost diagnosis of genetic abnormalities from fixed miscarriage and stillborn pregnancies. In: A focus on Genomics: 21st Annual Conference on the Organisation and Expression of the Genome. The Genome Conference 2000, Lorne, Victoria, Australia, (122-122). 13 - 17 February 2000. 62  
Biros, I., Poetter, K., Findlay, I. and Mitchelson, K. (2000). Paramagnetic beads technology in high through-put DNA template processing. In: A focus on Genomics: 21st Annual Conference on the Organisation and Expression of the Genome. The Genome Conference 2000, Lorne, Victoria, Australia, (91-91). 13 - 17 February 2000. 44  
Irwin, D.L., Bryan, J.L., Chan, F.Y., Matthews, P.L., Healey, S.C., Peters, M. and Findlay, I. (2003) Prenatal diagnosis of tetrasomy 18p using multiplex fluorescent PCR and comparison with a variety of techniques. Genetic Testing, 7 1: 1-6. doi:10.1089/109065703321560868 62   6 Cited 5 times in Scopus5 0
Findlay, I., Matthews, P., Biros, I., Mitchelson, K., Chan, F-Y. and Forbes, K. L. (2000). Same day and inexpensive prenatal diagnosis of trisomies 21, 18 and 13 from amniotic fluid. In: A focus on Genomics: 21st Annual Conference on the Organisation and Expression of the Genome. The Genome Conference 2000, Lorne, Victoria, Australia, (123-123). 13 - 17 February 2000. 61  
Findlay, I., Forbes, K. L. and Parker, M. H. (2000) Screening gamete donors for cystic fibrosis status. Medical Journal of Australia, 173 7: 380-381. 55   2
Mitchelson, K., Davis, J., Biros, I. and Findlay, I. (2000). Sequencing of RAPD fragments using 3-extended oligonucleotide primers by capillary array electrophoresis. In: A focus on Genomics: 21st Annual Conference on the Organisation and Expression of the Genome. The Genome Conference 2000, Lorne, Victoria, Australia, (179-179). 13 - 17 February 2000. 45  
Aung, H. T., Harrison, D. K., Findlay, I., Mattick, J. S., Martin, N. and Carroll, B. J. (2002). Stringent genetic programming of DNA methylation in humans. In: Australian Human Gene Mapping Meeting, Hobart, (). 4-6 December, 2002. 62  
Findlay, I., Matthews, P. L., Mulcahy, B. K. and Mitchelson, K. (2001) Using MF-PCR to diagnose multiple defects from single cells: implications for PGD. Molecular and Cellular Endocrinology, 183 Supp. 1: S5-S12. doi:10.1016/S0303-7207(01)00567-6 37   9 Cited 8 times in Scopus8 0
Aung, H. T., Carroll, B. J., Findlay, I., Harrison, D. and Waldron, J. (2002). Widespread tissue-specific DNA methylation polymorphisms in humans. In: The Genome Conference. The Genome Conference, Lorne, ((Poster)). 17-21 February, 2002. 50