A case of maternity testing: Exclusion by polymorphic VNTR markers of DNA
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical)
Link
http://www.nature.com/articles/jhg199036.pdf
Reference9 articles.
1. Akane, A., Matsubara, K., Shiono, H., Yuasa, I., Yokota, S., Yamada, M. and Nakagome, Y. 1990. Paternity testing: blood group systems and DNA analysis by VNTR markers.J. Forensic Sci. 35: 1217–1225.
2. Jeffreys, A.J., Royle, N.J., Wilson, V. and Wong, Z. 1988. Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA.Nature 332: 278–281.
3. Nakamura, Y., Leppert, M., O'Connell, P., Wolff, R., Holm, T., Culver, M., Martin, C., Fujimoto, E., Hoff, M., Kumkin, E. and White, R. 1987a. Variable number of tandem repeat (VNTR) markers for human gene mapping.Science 235: 1616–1622.
4. Nakamura, Y., Gillilan, S., O'Connel, P., Leppert, M., Lathrop, G.M., Lalouel, J.-M. and White, R. 1987b. Isolation and mapping of a polymorphic DNA sequence pYNH24 on chromosome 2 (D2S44).Nucleic Acids Res. 15: 10073.
5. Nakamura, Y., Fujimoto, E., O'Connel, P., Leppert, M., Lathrop, G.M., Lalouel, J.-M. and White, R. 1987c. Isolation and mapping of a polymorphic DNA sequence (pEFD126.3) on chromosome 9q (D9S7).Nucleic Acids Res. 15: 10607.
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1. Sex determination of forensic samples by dual PCR amplification of an X-Y homologous gene;Forensic Science International;1992-01
2. Carrier diagnosis by RFLP analysis in a family affected with infantile hypophosphatasia: Case report;Japanese Journal of Human Genetics;1991-12
3. Diagnosis of twin zygosity by hypervariable RFLP markers;American Journal of Medical Genetics;1991
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