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Volumn 150, Issue 1, 2005, Pages 17-21

Pros and cons in the use of SNPs in forensic kinship investigation: A comparative analysis with STRs

Author keywords

Kinship; Mutation; Null allele; SNP; STR

Indexed keywords

ARTICLE; COMPARATIVE STUDY; GENE MUTATION; MUTATION RATE; PATERNITY TEST; PRIORITY JOURNAL; SHORT TANDEM REPEAT; SIMULATION; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL ANALYSIS;

EID: 17144376705     PISSN: 03790738     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.forsciint.2004.06.018     Document Type: Article
Times cited : (129)

References (12)
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    • A.S. Kondrashov Direct estimates of human per nucleotide mutation rates at 20 loci causing Mendelian diseases Hum. Mutat. 21 2003 12 27
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    • Kondrashov, A.S.1
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    • An assessment of the utility of single nucleotide polymorphisms (SNPs) for forensic purposes
    • P. Gill An assessment of the utility of single nucleotide polymorphisms (SNPs) for forensic purposes Int. J. Legal Med. 114 2001 204 210
    • (2001) Int. J. Legal Med. , vol.114 , pp. 204-210
    • Gill, P.1
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    • Amorim, A.1    Rocha, J.2
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    • VWA STR genotyping: Further inconsistencies between Perkin-Elmer and Promega kits
    • C. Alves, A. Amorim, L. Gusmão, and L. Pereira VWA STR genotyping: further inconsistencies between Perkin-Elmer and Promega kits Int. J. Legal Med. 115 2001 97 99
    • (2001) Int. J. Legal Med. , vol.115 , pp. 97-99
    • Alves, C.1    Amorim, A.2    Gusmão, L.3    Pereira, L.4
  • 9
    • 0037764728 scopus 로고    scopus 로고
    • Identification of a D8S1179 primer binding site mutation and the validation of a primer designed to recover null alleles
    • C. Leibelt, B. Budowle, P. Collins, Y. Daoudi, T. Moretti, G. Nunn, D. Reeder, and R. Roby 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    Reeder, D.7    Roby, R.8
  • 10
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    • Human SNP variability and mutation rate are higher in regions of high recombination
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.