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Volumn 111, Issue 4-5, 2002, Pages 468-469

Genomic evidence versus characterisation of a single (17;22) translocation on NF1 gene duplication: Lessons from deletions in "balance" chromosomal rearrangements. Reply

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NUCLEAR FACTOR I;

EID: 0036820731     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-002-0795-2     Document Type: Letter
Times cited : (2)

References (13)
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  • 2
    • 0034897565 scopus 로고    scopus 로고
    • Identification of duplicated genes in 17q11.2 using FISH on stretched chromosomes and DNA fiber
    • Ventivegna A, Venturin M, Gervasini C, Corrado L, Larizza L, Riva P (2001) Identification of duplicated genes in 17q11.2 using FISH on stretched chromosomes and DNA fiber. Hum Genet 109:48-54
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    • Ventivegna, A.1    Venturin, M.2    Gervasini, C.3    Corrado, L.4    Larizza, L.5    Riva, P.6
  • 7
    • 0035500899 scopus 로고    scopus 로고
    • Recent duplication, domain accretion and the dynamic mutation of the human genome
    • Eichler EE (2001) Recent duplication, domain accretion and the dynamic mutation of the human genome. Trends Genet 117:661-669
    • (2001) Trends Genet , vol.117 , pp. 661-669
    • Eichler, E.E.1
  • 8
    • 0036556292 scopus 로고    scopus 로고
    • Tandem duplication of the NF1 gene detected by high-resolution FISH in the duplicon-rich 17q11.2 region
    • Gervasini C, Bentivegna A, Venturin M, Corrado L, Larizza L, Riva P (2002) Tandem duplication of the NF1 gene detected by high-resolution FISH in the duplicon-rich 17q11.2 region. Hum Genet 110:314-321
    • (2002) Hum Genet , vol.110 , pp. 314-321
    • Gervasini, C.1    Bentivegna, A.2    Venturin, M.3    Corrado, L.4    Larizza, L.5    Riva, P.6
  • 9
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    • Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion
    • Giacalone JP, Franck U (1992) Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion. Am J Hum Gent 51:226
    • (1992) Am J Hum Gent , vol.51 , pp. 226
    • Giacalone, J.P.1    Franck, U.2
  • 10
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    • Molecular characterization and gene content of breakpoint boundaries in patients with Neurofibromatosis type 1 with 17q11.2 microdeletions
    • Jenne DE, Tinschert S, Reimann H, Lasinger W, Thiel G, Hameister H, Kehrer-Sawatzki H (2001) Molecular characterization and gene content of breakpoint boundaries in patients with Neurofibromatosis type 1 with 17q11.2 microdeletions. Am J Hum Genet 69:516-527
    • (2001) Am J Hum Genet , vol.69 , pp. 516-527
    • Jenne, D.E.1    Tinschert, S.2    Reimann, H.3    Lasinger, W.4    Thiel, G.5    Hameister, H.6    Kehrer-Sawatzki, H.7
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    • High resolution commparative genomic hybridisation in clinical cytogenetics
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    • Kirchhoff, M.1    Rose, H.2    Lundtseen, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.