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Volumn 39, Issue SUPPL. 1, 2011, Pages

FINDbase: A worldwide database for genetic variation allele frequencies updated

Author keywords

[No Author keywords available]

Indexed keywords

DRUG METABOLIZING ENZYME;

EID: 78651340989     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkq1236     Document Type: Article
Times cited : (19)

References (21)
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    • Patrinos, G.P. (2006) National and Ethnic Mutation databases: Documenting populations' genography. Hum. Mutat., 27, 879-887.
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    • Patrinos, G.P.1
  • 2
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    • Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders
    • Hamosh, A., Scott, A.F., Amberger, J., Bocchini, C.and McKusick, V.A. (2005) Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders. Nucleic Acids Res., 33, D514-D517.
    • (2005) Nucleic Acids Res. , vol.33
    • Hamosh, A.1    Scott, A.F.2    Amberger, J.3    Bocchini, C.4    McKusick, V.A.5
  • 4
    • 78650488246 scopus 로고    scopus 로고
    • Locus-specific database domain and data content analysis: Evolution and content maturation towards clinical use
    • Mitropoulou, C., Webb, A.J., Mitropoulos, K., Brookes, A.J.and Patrinos, G.P. (2010) Locus-specific database domain and data content analysis: Evolution and content maturation towards clinical use. Hum. Mutat., 31, 1109-1116.
    • (2010) Hum. Mutat. , vol.31 , pp. 1109-1116
    • Mitropoulou, C.1    Webb, A.J.2    Mitropoulos, K.3    Brookes, A.J.4    Patrinos, G.P.5
  • 6
    • 0036258208 scopus 로고    scopus 로고
    • Cystic fibrosis: A worldwide analysis of CFTR mutations- correlation with incidence data and application to screening
    • Bobadilla, J.L., Macek, M., Jr, Fine, J.P.and Farrell, P.M. (2002) Cystic fibrosis: A worldwide analysis of CFTR mutations- correlation with incidence data and application to screening. Hum. Mutat., 19, 575-606.
    • (2002) Hum. Mutat. , vol.19 , pp. 575-606
    • Bobadilla, J.L.1    Macek Jr., M.2    Fine, J.P.3    Farrell, P.M.4
  • 8
    • 0347125141 scopus 로고    scopus 로고
    • Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies
    • Patrinos, G.P., Giardine, B., Riemer, C., Miller, W., Chui, D.H., Anagnou, N.P., Wajcman, H.and Hardison, R.C. (2004) Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. Nucleic Acids Res., 32, D537-D541.
    • (2004) Nucleic Acids Res. , vol.32
    • Patrinos, G.P.1    Giardine, B.2    Riemer, C.3    Miller, W.4    Chui, D.H.5    Anagnou, N.P.6    Wajcman, H.7    Hardison, R.C.8
  • 12
    • 77955616931 scopus 로고    scopus 로고
    • Genetic database and their potential in pharmacogenomics
    • Lagoumintzis, G., Poulas, K.and Patrinos, G.P. (2010) Genetic database and their potential in pharmacogenomics. Curr. Pharm. Des., 16, 2224-2231.
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    • Eckerson, W.W.1
  • 16
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    • Patrinos, G.P.and Petricoin, E.F. (2009) A new scientific journal linked to a genetic database: Towards a novel publication modality. Hum. Genomics Proteomics, 1, e597478.
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  • 17
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    • DNA, diseases and databases: Disastrously deficient
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.