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Volumn 6, Issue 3, 1996, Pages 218-225

Construction of a 750-kb bacterial clone contig and restriction map in the region of human chromosome 21 containing the progressive myoclonus epilepsy gene

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ARTICLE; BACTERIOPHAGE P1; CHROMOSOME 21Q; COSMID; GENE LINKAGE DISEQUILIBRIUM; GENETIC RECOMBINATION; HUMAN; HUMAN CELL; MOLECULAR CLONING; MYOCLONUS EPILEPSY; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RESTRICTION MAPPING; YEAST ARTIFICIAL CHROMOSOME;

EID: 19144369837     PISSN: 10549803     EISSN: None     Source Type: Journal    
DOI: 10.1101/gr.6.3.218     Document Type: Article
Times cited : (41)

References (15)
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    • Disease gene mapping in isolated human populations: The example of Finland
    • de la Chapelle, A. 1993. Disease gene mapping in isolated human populations: The example of Finland. J. Med. Genet. 30: 857-865.
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    • De La Chapelle, A.1
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    • Isolation of cDNAs to a region poorly represented in the CEPH chromosome 21 YAC contig: Candidate genes for genetic diseases mapped to 21q22.3
    • Gardiner, K., H. Ichikawa, M. Ohki, D. Patterson, and J.-F. Feng. 1995. Isolation of cDNAs to a region poorly represented in the CEPH chromosome 21 YAC contig: Candidate genes for genetic diseases mapped to 21q22.3. Genomics 30: 376-379.
    • (1995) Genomics , vol.30 , pp. 376-379
    • Gardiner, K.1    Ichikawa, H.2    Ohki, M.3    Patterson, D.4    Feng, J.-F.5
  • 5
    • 0027184311 scopus 로고
    • A Not I restriction map of the entire long arm of human chromosome 21
    • Ichikawa H., F. Hosoda, Y. Arai, K. Shimizu, M. Ohira, and M. Ohki. 1993. A Not I restriction map of the entire long arm of human chromosome 21. Nature Genet. 4: 361-366.
    • (1993) Nature Genet. , vol.4 , pp. 361-366
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  • 6
    • 0029118590 scopus 로고
    • A 405-kb cosmid contig and HindIII restriction map of the progressive myoclonus epilepsy type 1 (EPM1) candidate region in 21q22.3
    • Lafreniere, R.G., P.J. De Jong, and G.A. Rouleau. 1995. A 405-kb cosmid contig and HindIII restriction map of the progressive myoclonus epilepsy type 1 (EPM1) candidate region in 21q22.3. Genoinics 29: 288-290.
    • (1995) Genoinics , vol.29 , pp. 288-290
    • Lafreniere, R.G.1    De Jong, P.J.2    Rouleau, G.A.3
  • 9
    • 0027430115 scopus 로고
    • Progressive myoclonus epilepsy of Unverricht-Lundborg type: A clinical and molecular genetic study of a family from the United States with four affected sibs
    • Lehesjoki, A.-E., R. Eldridge, J. Eldridge, B.J. Wilder, and A. de la Chapelle. 1993a. Progressive myoclonus epilepsy of Unverricht-Lundborg type: A clinical and molecular genetic study of a family from the United States with four affected sibs. Neurology 43: 2384-2386.
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    • Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: Linkage disequilibrium allows high resolution mapping
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.