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Volumn 146, Issue 1, 2003, Pages 70-72

Does conventional cytogenetics detect the real frequency of 19q13 aberrations in benign thyroid lesions? A survey of 38 cases

Author keywords

[No Author keywords available]

Indexed keywords

ACCURACY; ARTICLE; CHROMOSOME; CHROMOSOME ABERRATION; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FREQUENCY; GENE PROBE; GENE STRUCTURE; GENE TRANSLOCATION; GOITER; HUMAN; HUMAN CELL; HUMAN TISSUE; KARYOTYPE; MALE; MOLECULAR CLONING; PRIORITY JOURNAL; TELOMERE; THYROID ADENOMA;

EID: 0141676610     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(03)00131-6     Document Type: Article
Times cited : (3)

References (13)
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  • 5
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    • Nonpalpable thyroid nodules: Managing an epidemic
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    • Ross D.S. Nonpalpable thyroid nodules: managing an epidemic. [Editorial] J Clin Endocrinol Metab. 87:2002;1938-1940.
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    • Ross, D.S.1
  • 6
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    • A cryptic t(5;11)(q35;p11.5) in 2 children with acute myeloid leukemia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assay
    • Brown J., Jawad M., Twigg S.R.F., Saracoglu K., Sauerbrey A., Thomas A.E., Eils R., Harbott J., Kearney L. A cryptic t(5;11)(q35;p11.5) in 2 children with acute myeloid leukemia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assay. Blood. 99:2002;2526-2531.
    • (2002) Blood , vol.99 , pp. 2526-2531
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  • 7
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    • Detection of a cryptic translocation t(13;20)(q34;p13) in an unexplained case of MCA/MR: Value of FISH over high resolution banding
    • de Die-Smulders C.E., Engelen J.J., Albrechts J.C., Hamers G.J. Detection of a cryptic translocation t(13;20)(q34;p13) in an unexplained case of MCA/MR: value of FISH over high resolution banding. Am J Med Genet. 86:1999;385-388.
    • (1999) Am J Med Genet , vol.86 , pp. 385-388
    • De Die-Smulders, C.E.1    Engelen, J.J.2    Albrechts, J.C.3    Hamers, G.J.4
  • 8
    • 0034786240 scopus 로고    scopus 로고
    • Frequent gain of chromosome 19 in megakaryoblastic leukemias detected by comparative genomic hybridization
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    • (2002) Genes Chromosomes Cancer , vol.2 , pp. 285-293
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  • 10
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    • Third report of t(19q)(13.4) in mesenchymal hamartoma of the liver with comments on link to embryonal sarcoma
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  • 11
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    • Mascarello J.T., Krous H.F. Second report of a translocation involving 19q13.4 in a mesenchymal hamartoma of the liver. Cancer Genet Cytogenet. 58:1992;141-142.
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  • 13
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    • Translocation t(5;19): A recurrent change in thyroid follicular adenoma
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.