DNA variations in human and medical genetics: 25 years of my experience

Author:

Nakamura Yusuke

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference143 articles.

1. Botstein, D., White, R. L., Skolnick, M. & Davis, R. W. Construction of a genetic linkage map in man using restriction fragment length polymorphisms. Am. J. Hum. Genet. 32, 314–331 (1980).

2. Nakamura, Y., Leppert, M., O’Connell, P., Wolff, R., Holm, T., Culver, M. et al. Variable number of tandem repeat (VNTR) markers for human gene mapping. Science 235, 1616–1622 (1987).

3. Jeffreys, A. J., Wilson, V. & Thein, S. L. Hypervariable ‘minisatellite’ regions in human DNA. Nature (London) 314, 67–73 (1985).

4. Odelberg, S. J., Plaetke, R., Eldridge, J. R., Ballard, L., O’Connell, P., Nakamura, Y. et al. Characterization of eight VNTR loci by agarose gel electrophoresis: Implications for parentage testing and forensic individualization. Genomics 5, 915–924 (1989).

5. Gatti, R., Nakamura, Y., Nussmeier, M., Susi, E., Shan, W. & Grody, W. Informativeness of VNTR genetic markers for detecting chimerism after bone marrow transplantation. Disease Markers 7, 105–112 (1989).

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