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Volumn 111, Issue 4-5, 2002, Pages 465-467

Molecular characterisatin of t(17;22)(q11.2;q11.2) is not consistent with NF1 gene duplication

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 17Q; CHROMOSOME TRANSLOCATION; DNA FLANKING REGION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DUPLICATION; GENE PROBE; HETEROZYGOTE; HUMAN; LETTER; METAPHASE CHROMOSOME; MOLECULAR GENETICS; NEUROFIBROMATOSIS; PRIORITY JOURNAL; TANDEM REPEAT; VARIABLE NUMBER OF TANDEM REPEAT; CHROMOSOME 17; CHROMOSOME 22; GENE TRANSLOCATION; GENETICS; NOTE; TUMOR SUPPRESSOR GENE;

EID: 0036781403     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-002-0794-3     Document Type: Letter
Times cited : (8)

References (7)
  • 2
    • 0036556292 scopus 로고    scopus 로고
    • Tandem duplication of the NF1 gene detected by high-resolution FISH in the 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 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
  • 4
    • 0034892401 scopus 로고    scopus 로고
    • 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
  • 5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.