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Volumn 3, Issue 1, 1993, Pages 13-22

Automated DMA profiling employing multiplex amplification of short tandem repeat loci

Author keywords

[No Author keywords available]

Indexed keywords

FLUORESCENT DYE; REPETITIVE DNA;

EID: 0027184458     PISSN: 10889051     EISSN: None     Source Type: Journal    
DOI: 10.1101/gr.3.1.13     Document Type: Article
Times cited : (331)

References (11)
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    • Beckmann, J.S.1    Weber, J.L.2
  • 2
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    • Edwards, A., A. Civitello, H.A. Hammond, and C.T. Caskey. 1991. DNA typing and genetic mapping with trimeric and tetrameric tandem repeats. Am. J. Hum. Genet. 49: 746-756.
    • (1991) Am. J. Hum. Genet. , vol.49 , pp. 746-756
    • Edwards, A.1    Civitello, A.2    Hammond, H.A.3    Caskey, C.T.4
  • 3
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    • The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome
    • Economou, E.P., A.W. Bergen, A.C. Warren, and S.E. Antonarakis. 1990. The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome. Proc. Natl. Acad. Sci. 87: 2951-2954.
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    • Economou, E.P.1    Bergen, A.W.2    Warren, A.C.3    Antonarakis, S.E.4
  • 4
    • 0025744382 scopus 로고
    • Predictive diagnosis of myotonic dystrophy with flanking microsatellite markers
    • Mully, J.C., A.K. Gedeon, S.J. White, E.A. Haan, and R.I. Richards. 1991. Predictive diagnosis of myotonic dystrophy with flanking microsatellite markers. J. Med. Genet. 28: 448-452.
    • (1991) J. Med. Genet. , vol.28 , pp. 448-452
    • Mully, J.C.1    Gedeon, A.K.2    White, S.J.3    Haan, E.A.4    Richards, R.I.5
  • 5
    • 0026779977 scopus 로고
    • Multiplex PCR amplification of three microsatellites within the CFTR gene
    • Morral, N. and X. Estivill. 1992. Multiplex PCR amplification of three microsatellites within the CFTR gene. Genomics 13:1362-1364.
    • (1992) Genomics , vol.13 , pp. 1362-1364
    • Morral, N.1    Estivill, X.2
  • 6
    • 0026343294 scopus 로고
    • Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombination
    • Oudet, C., R. Heilig, A. Hanauer, and J.-L. Mandel. 1991. Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombination. Am. J. Hum. Genet. 49: 311-319.
    • (1991) Am. J. Hum. Genet. , vol.49 , pp. 311-319
    • Oudet, C.1    Heilig, R.2    Hanauer, A.3    Mandel, J.-L.4
  • 7
    • 0026950914 scopus 로고
    • Delineation of a 50 kilobase segment containing the recombination site in a sporadic case of Huntington's disease
    • Weber, B., O. Riess, G. Wolff, S. Andrew, C. Collins, R. Graham, J. Thielman, and M.R. Hayden. 1992. Delineation of a 50 kilobase segment containing the recombination site in a sporadic case of Huntington's disease. Nature Genet. 2: 216-222.
    • (1992) Nature Genet. , vol.2 , pp. 216-222
    • Weber, B.1    Riess, O.2    Wolff, G.3    Andrew, S.4    Collins, C.5    Graham, R.6    Thielman, J.7    Hayden, M.R.8
  • 10
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    • Androgen receptor gene mutations in X-linked spinal and bulbar muscular atropy
    • La Spada, A.R., E.M. Wilson, D.B. Lubahn, A.E. Harding, and K.H. Fischbeck. 1991. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atropy. Nature 352: 77-79.
    • (1991) Nature , vol.352 , pp. 77-79
    • La Spada, A.R.1    Wilson, E.M.2    Lubahn, D.B.3    Harding, A.E.4    Fischbeck, K.H.5
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    • Richards, R.I. and G.R. Sutherland. 1992. Fragile X syndrome: The molecular picture comes into focus. Trends Genet. 8: 249-253.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.