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Volumn 12, Issue 2, 2010, Pages 94-96

A silent allele in the locus D19S433 contained within the AmpFℓSTR® Identifiler™ PCR Amplification Kit

Author keywords

D19S433; Paternity test; Short tandem repeat; Silent allele; Single locus mismatch

Indexed keywords

DNA;

EID: 76849106453     PISSN: 13446223     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.legalmed.2009.12.002     Document Type: Article
Times cited : (21)

References (7)
  • 1
    • 20644445861 scopus 로고    scopus 로고
    • Analysis of a paternity case in which the alleged father was deceased: single locus mismatch
    • Tsuji A., Ishiko A., Inoue H., Kudo K., and Ikeda N. Analysis of a paternity case in which the alleged father was deceased: single locus mismatch. Fukuoka Acta Med 96 3 (2005) 76-80
    • (2005) Fukuoka Acta Med , vol.96 , Issue.3 , pp. 76-80
    • Tsuji, A.1    Ishiko, A.2    Inoue, H.3    Kudo, K.4    Ikeda, N.5
  • 2
    • 50449109860 scopus 로고    scopus 로고
    • A D19S433 primer binding site mutation and the frequency in Japanese of the silent allele it causes
    • Mizuno N., Kitayama T., Fujii K., Nakahara H., Yoshida K., Sekiguchi K., et al. A D19S433 primer binding site mutation and the frequency in Japanese of the silent allele it causes. J Forensic Sci 53 5 (2008) 1-6
    • (2008) J Forensic Sci , vol.53 , Issue.5 , pp. 1-6
    • Mizuno, N.1    Kitayama, T.2    Fujii, K.3    Nakahara, H.4    Yoshida, K.5    Sekiguchi, K.6
  • 3
    • 34548408534 scopus 로고    scopus 로고
    • Identification of a rare mutation in a TH01 primer binding site
    • Takayama T., Takada N., Suzuki R., Nagaoka S., and Watanabe Y. Identification of a rare mutation in a TH01 primer binding site. Leg Med 9 6 (2007) 289-292
    • (2007) Leg Med , vol.9 , Issue.6 , pp. 289-292
    • Takayama, T.1    Takada, N.2    Suzuki, R.3    Nagaoka, S.4    Watanabe, Y.5
  • 4
    • 0037764728 scopus 로고    scopus 로고
    • Identification of a D8S1179 primer binding site mutation and the validation of a primer designed to recover null alleles
    • Leibelt C., Budowle B., Collins P., Daoudi Y., Moretti T., Nunn G., et al. Identification of a D8S1179 primer binding site mutation and the validation of a primer designed to recover null alleles. Forensic Sci Int 133 (2003) 220-227
    • (2003) Forensic Sci Int , vol.133 , pp. 220-227
    • Leibelt, C.1    Budowle, B.2    Collins, P.3    Daoudi, Y.4    Moretti, T.5    Nunn, G.6
  • 5
    • 33847116660 scopus 로고    scopus 로고
    • A single mutation in the FGA locus responsible for false homozygosities and discrepancies between commercial kits in an unusual paternity test case
    • Ricci U., Melean G., Robino C., and Genuardi M. A single mutation in the FGA locus responsible for false homozygosities and discrepancies between commercial kits in an unusual paternity test case. J Forensic Sci 52 2 (2007) 393-396
    • (2007) J Forensic Sci , vol.52 , Issue.2 , pp. 393-396
    • Ricci, U.1    Melean, G.2    Robino, C.3    Genuardi, M.4
  • 6
    • 1042264307 scopus 로고    scopus 로고
    • Primer binding site mutations affecting the typing of STR loci contained within the AmpFℓSTR® SGM Plus™ kit
    • Clayton T.M., Hill S.M., Denton L.A., Watson S.K., and Urquhart A.J. Primer binding site mutations affecting the typing of STR loci contained within the AmpFℓSTR® SGM Plus™ kit. Forensic Sci Int 139 (2004) 255-259
    • (2004) Forensic Sci Int , vol.139 , pp. 255-259
    • Clayton, T.M.1    Hill, S.M.2    Denton, L.A.3    Watson, S.K.4    Urquhart, A.J.5
  • 7
    • 34249049573 scopus 로고    scopus 로고
    • Identification and sequence analysis of discordant phenotypes between AmpFℓSTR® SGM Plus™ and PowerPlex® 16
    • Vanderheyden N., Mai A., Gilissen A., Cassiman J.J., and Decorte R. Identification and sequence analysis of discordant phenotypes between AmpFℓSTR® SGM Plus™ and PowerPlex® 16. Int J Legal Med 121 (2007) 297-301
    • (2007) Int J Legal Med , vol.121 , pp. 297-301
    • Vanderheyden, N.1    Mai, A.2    Gilissen, A.3    Cassiman, J.J.4    Decorte, R.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.