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Volumn 36, Issue 8, 1998, Pages 523-527

Population genomics: Laying the groundwork for genetic disease modeling and targeting

Author keywords

[No Author keywords available]

Indexed keywords

CONFERENCE PAPER; DATA BASE; FAMILY; GENEALOGY; GENETIC DISORDER; GENETIC MODEL; GENETIC PREDISPOSITION; GENOTYPE; GOVERNMENT; HUMAN; ICELAND; PHENOTYPE; POPULATION GENETICS; PREVENTIVE MEDICINE; PRIORITY JOURNAL; PUBLIC HEALTH SERVICE;

EID: 0031672085     PISSN: 14346621     EISSN: None     Source Type: Journal    
DOI: 10.1515/CCLM.1998.089     Document Type: Conference Paper
Times cited : (103)

References (12)
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    • Clinical and pathological features of an autosomal dominant adult-onset leukodystrophy simulating chronic progressive multiple sclerosis
    • Schwankhaus JD, Katz DA, Eldridge R, Schlesinger S, McFarland H. Clinical and pathological features of an autosomal dominant adult-onset leukodystrophy simulating chronic progressive multiple sclerosis. Arch. Neurol. 1994; 51:757-66.
    • (1994) Arch Neurol , vol.51 , pp. 757-766
    • Schwankhaus, J.D.1    Katz, D.A.2    Eldridge, R.3    Schlesinger, S.4    McFarland, H.5
  • 2
    • 0027458051 scopus 로고    scopus 로고
    • Insulin resistance and insulin deficiency in the pathogenesis of type 2 (non-insulin dependent) diabetes mellitus: Errors of metabolism or of methods
    • Groop LC, Widen E, Ferrannini E. Insulin resistance and insulin deficiency in the pathogenesis of type 2 (non-insulin dependent) diabetes mellitus: errors of metabolism or of methods. Diabetologia 36:1326-1331.
    • Diabetologia , vol.36 , pp. 1326-1331
    • Groop, L.C.1    Widen, E.2    Ferrannini, E.3
  • 6
    • 0021706934 scopus 로고
    • Abnormal metabolism of gamma-trace alkaline microprotein. The basic defect in hereditary cerebral hemorrhage with amyloidosis
    • Grubb A, Jensson O, Gudmundsson G, Arnason A, Lofberg H, Malm J. Abnormal metabolism of gamma-trace alkaline microprotein. The basic defect in hereditary cerebral hemorrhage with amyloidosis. N Engl J Med 1984; 311:1547-9.
    • (1984) N Engl J Med , vol.311 , pp. 1547-1549
    • Grubb, A.1    Jensson, O.2    Gudmundsson, G.3    Arnason, A.4    Lofberg, H.5    Malm, J.6
  • 8
    • 0026718486 scopus 로고
    • Hereditary cystatin C amyloid angiopathy: Identification of the disease-causing mutation and specific diagnosis by polymerase chain reaction based analysis
    • Abrahamson M, Jonsdottir S, Olafsson I, Jensson O, Grubb A. Hereditary cystatin C amyloid angiopathy: Identification of the disease-causing mutation and specific diagnosis by polymerase chain reaction based analysis. Hum Genet 1992: 89:377-80.
    • (1992) Hum Genet , vol.89 , pp. 377-380
    • Abrahamson, M.1    Jonsdottir, S.2    Olafsson, I.3    Jensson, O.4    Grubb, A.5
  • 10
    • 0030725721 scopus 로고    scopus 로고
    • A gene (ETM) for essential tremor maps to chromosome 2p22-p25
    • Higgins JJ, Pho LT, Nee LE. A gene (ETM) for essential tremor maps to chromosome 2p22-p25. Movement Disorders 1997; 12:859-64.
    • (1997) Movement Disorders , vol.12 , pp. 859-864
    • Higgins, J.J.1    Pho, L.T.2    Nee, L.E.3
  • 11
    • 0344564553 scopus 로고    scopus 로고
    • http://www-leland.stanford.edu/group/morrinst/Protocol.html
  • 12
    • 0030728925 scopus 로고    scopus 로고
    • Allele sharing models: LOD scores and accurate linkage tests
    • Kong A, Cox NJ. Allele sharing models: LOD scores and accurate linkage tests. Am J Hum Genet 1997; 61:1179-88.
    • (1997) Am J Hum Genet , vol.61 , pp. 1179-1188
    • Kong, A.1    Cox, N.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.