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Volumn 37, Issue 2, 2009, Pages 438-440

PCR in forensic genetics

Author keywords

DNA analysis; Forensic genetics; Identity testing; PCR; Short tandem repeat (STR); Single nucleotide polymorphism (SNP)

Indexed keywords

CYTOCHROME P450 2C9; MELANOCORTIN 1 RECEPTOR; MITOCHONDRIAL DNA; DNA;

EID: 65549089579     PISSN: 03005127     EISSN: 14708752     Source Type: Journal    
DOI: 10.1042/BST0370438     Document Type: Review
Times cited : (22)

References (13)
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    • (1985) Nature , vol.316 , pp. 76-79
    • Jeffreys, A.J.1    Wilson, V.2    Thein, S.L.3
  • 3
    • 0242581339 scopus 로고
    • Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus
    • Gyllensten, U.B. and Ehrlich, H.A. (1988) Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus. Proc. Natl. Acad. Sci. U.S.A. 85, 7652-7656
    • (1988) Proc. Natl. Acad. Sci. U.S.A , vol.85 , pp. 7652-7656
    • Gyllensten, U.B.1    Ehrlich, H.A.2
  • 5
    • 0027184458 scopus 로고
    • Automated DNA profiling employing multiplex amplification of short tandem repeat loci
    • Kimpton, C.P., Gill, P., Walton, A., Urquhart, A., Millican, E.S. and Adams, M. (1993) Automated DNA profiling employing multiplex amplification of short tandem repeat loci. PCR Methods Appl. 3, 13-22
    • (1993) PCR Methods Appl , vol.3 , pp. 13-22
    • Kimpton, C.P.1    Gill, P.2    Walton, A.3    Urquhart, A.4    Millican, E.S.5    Adams, M.6
  • 6
    • 0035055939 scopus 로고    scopus 로고
    • An assessment of the utility of single nucleotide polymorphisms (SNPs) for forensic purposes
    • Gill, P. (2001) An assessment of the utility of single nucleotide polymorphisms (SNPs) for forensic purposes. Int. J. Legal Med. 114, 204-210
    • (2001) Int. J. Legal Med , vol.114 , pp. 204-210
    • Gill, P.1
  • 9
    • 56549084702 scopus 로고    scopus 로고
    • Typing of 48 autosomal SNPs and amelogenin with GenPlex SNP genotyping system in forensic genetics
    • Tomas, C., Stangegaard, M., Børsting, C., Hansen, A.J. and Morling, N. (2008) Typing of 48 autosomal SNPs and amelogenin with GenPlex SNP genotyping system in forensic genetics. Forensic Sci. Int. 3, 1-6
    • (2008) Forensic Sci. Int , vol.3 , pp. 1-6
    • Tomas, C.1    Stangegaard, M.2    Børsting, C.3    Hansen, A.J.4    Morling, N.5
  • 12
    • 39549097952 scopus 로고    scopus 로고
    • Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression
    • Eiberg, H., Troelsen, J., Nielsen, M., Mikkelsen, A., Mengel-From, J., Kjaer, K.W. and Hansen, L. (2008) Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression. Hum. Genet. 123, 177-187
    • (2008) Hum. Genet , vol.123 , pp. 177-187
    • Eiberg, H.1    Troelsen, J.2    Nielsen, M.3    Mikkelsen, A.4    Mengel-From, J.5    Kjaer, K.W.6    Hansen, L.7
  • 13
    • 50849137155 scopus 로고    scopus 로고
    • The SNPforID browser: An online tool for query and display of frequency data from the SNPforID project
    • Amigo, J., Phillips, C., Lareu, M. and Carracedo, A. (2008) The SNPforID browser: an online tool for query and display of frequency data from the SNPforID project. Int. J. Legal Med. 122, 435-440
    • (2008) Int. J. Legal Med , vol.122 , pp. 435-440
    • Amigo, J.1    Phillips, C.2    Lareu, M.3    Carracedo, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.