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American Biotechnology Laboratory
Volumn 15, Issue 3, 1997, Pages
Detection of point mutations using the minisequencing method
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[No Author keywords available]
Indexed keywords

EID: 2442571015     PISSN: 07493223     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (1)
References (4)
  • 1
    • 0025650533 scopus 로고
    • A primer-guided nucleotide incorporation assay in the genotyping of apolipoprotein E
    • Syvänen A-C, Aako-Setälä K, Harju L, Kontula K, Soderlund H. A primer-guided nucleotide incorporation assay in the genotyping of apolipoprotein E. Genomics 1990: 8:684-92.
    • (1990) Genomics , vol.8 , pp. 684-692
    • Syvänen, A.-C.1    Aako-Setälä, K.2    Harju, L.3    Kontula, K.4    Soderlund, H.5
  • 2
    • 0026580904 scopus 로고
    • Screening for defined cystic fibrosis mutations by solid-phase minisequencing
    • Jalanko A, Kere J, Savilahti E, et al. Screening for defined cystic fibrosis mutations by solid-phase minisequencing. Clin Chem 1992; 38:39-43.
    • (1992) Clin Chem , vol.38 , pp. 39-43
    • Jalanko, A.1    Kere, J.2    Savilahti, E.3
  • 3
    • 0027167679 scopus 로고
    • DNA diagnosis for the detection of sickle hemoglobinopathies
    • Steinberg MH. DNA diagnosis for the detection of sickle hemoglobinopathies. Am J Hematol 1993; 43:110-5.
    • (1993) Am J Hematol , vol.43 , pp. 110-115
    • Steinberg, M.H.1
  • 4
    • 0022372670 scopus 로고
    • Enzymatic amplification of β-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia
    • Saiki RK, Scarf S, Faloona K et al. Enzymatic amplification of β-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. Science 1985; 230:1350-4.
    • (1985) Science , vol.230 , pp. 1350-1354
    • Saiki, R.K.1    Scarf, S.2    Faloona, K.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.