Found 1 results
Filters: Author is D.-W. Xu  [Clear All Filters]
J. Zhang, Li, N., Lin, J. - Y., Li, Q., Hai, J., Xu, D. - W., and Qian, X. - L., Mitochondrial DNA mutations may not be frequent in patients with aplastic anemia - Genet. Mol. Res. 11 (3): 2130-2137 “Complete sequence analysis of mitochondrial DNA of aplastic anemia patients”, vol. 11. pp. 4668-4670, 2012.
Cui X, Liu F, Wang JQ, Zhang WJ, et al. (2012). Complete sequence analysis of mitochondrial DNA of aplastic anemia patients. Genet. Mol. Res. 11: 2130-2137. PMid:22911596   Pareek CS, Smoczynski R and Tretyn A (2011). Sequencing technologies and genome sequencing. J. Appl. Genet. 52: 413-435. PMid:21698376 PMCid:3189340   Porta M (2008). A Dictionary of Epidemiology. 5th edn. Oxford University Press, New York.   Rieder MJ, Taylor SL, Tobe VO and Nickerson DA (1998). Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome. Nucleic Acids Res. 26: 967-973. PMid:9461455 PMCid:147367   Wallace DC (2010). Mitochondrial DNA mutations in disease and aging. Environ. Mol. Mutagen. 51: 440-450. PMid:20544884