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Volumn 105, Issue 3, 1999, Pages 771-774

A case of myelofibrosis with a t(4;13)(q25;q12): Evidence for involvement of a second 13q12 locus in chronic myeloproliferative disorders

Author keywords

Chromosome 13; Chromosome 4; Myelofibrosis; Myeloproliferative

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 13Q; CHROMOSOME 4Q; CHROMOSOME TRANSLOCATION 13; CHROMOSOME TRANSLOCATION 4; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; MALE; MYELOFIBROSIS; PRIORITY JOURNAL;

EID: 0033001469     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1999.01414.x     Document Type: Article
Times cited : (6)

References (12)
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    • Gardiner, A.C., Corcoran, M.M. & Oscier, D.G. (1997) Cytogenetic, fluorescence in situ hybridisation, and clinical evaluation of translocations with concomitant deletion at 13q14 in chronic lymphocytic leukaemia. Genes, Chromosomes and Cancer, 20, 73-81.
    • (1997) Genes, Chromosomes and Cancer , vol.20 , pp. 73-81
    • Gardiner, A.C.1    Corcoran, M.M.2    Oscier, D.G.3
  • 4
    • 0029149080 scopus 로고
    • A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C)
    • Guilford, P., Dode, C., Crozet, F., Blanchard, S., Chaib, H., Levilliers, J., Levi-Acobas, F., Weil, D., Weissenbach, J., Cohen, D., Le Paslier, D., Kaplan, J.C. & Petit, C. (1995) A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C). Genomics, 29, 163-169.
    • (1995) Genomics , vol.29 , pp. 163-169
    • Guilford, P.1    Dode, C.2    Crozet, F.3    Blanchard, S.4    Chaib, H.5    Levilliers, J.6    Levi-Acobas, F.7    Weil, D.8    Weissenbach, J.9    Cohen, D.10    Le Paslier, D.11    Kaplan, J.C.12    Petit, C.13
  • 5
    • 0028869005 scopus 로고
    • A new myeloproliferative disorder associated with chromosomal translocations involving 8p11: A review
    • Macdonald, D.. Aguiar, R.C., Mason, P.J., Goldman, J.M. & Cross, N.C. (1995) A new myeloproliferative disorder associated with chromosomal translocations involving 8p11: a review, Leukemia, 9, 1628-1630.
    • (1995) Leukemia , vol.9 , pp. 1628-1630
    • Macdonald, D.1    Aguiar, R.C.2    Mason, P.J.3    Goldman, J.M.4    Cross, N.C.5
  • 6
    • 0029032790 scopus 로고
    • Karyotypic evolution in a granulocytic sarcoma developing in a myeloproliferative disorder with a novel (3;4) translocation
    • Myint, H., Chacko, J., Mould, S., Ross, F. & Oscier, D.G. (1995) Karyotypic evolution in a granulocytic sarcoma developing in a myeloproliferative disorder with a novel (3;4) translocation. British Journal of Haematology, 90, 462-464.
    • (1995) British Journal of Haematology , vol.90 , pp. 462-464
    • Myint, H.1    Chacko, J.2    Mould, S.3    Ross, F.4    Oscier, D.G.5
  • 7
    • 0028675056 scopus 로고
    • Construction of cosmid libraries from flow-sorted human chromosomes 1, 6, 7, 11, 13, and 18 for reference library resources
    • Nizetic, D., Monard, S., Young, B., Cotter, F., Zehetner, G. & Lehrach, H. (1994) Construction of cosmid libraries from flow-sorted human chromosomes 1, 6, 7, 11, 13, and 18 for reference library resources. Mammalian Genome, 5, 801-802.
    • (1994) Mammalian Genome , vol.5 , pp. 801-802
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  • 11
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    • Fine structure physical mapping of a 1-9 Mb region of chromosome 13q12
    • Still, I.H., Roberts, T. & Cowell. J.K. (1997) Fine structure physical mapping of a 1-9 Mb region of chromosome 13q12. Annals of Human Genetics, 61, 15-24.
    • (1997) Annals of Human Genetics , vol.61 , pp. 15-24
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  • 12
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    • Small cell variant of Ki-1 lymphoma associated with myelofibrosis and a novel constitutional chromosomal translocation t(3;4)(q13;q12)
    • Yeo, W., Wong, N., Chow, J., Tsoi, W.C., Johnson, P.J. & Wickham, N. (1996) Small cell variant of Ki-1 lymphoma associated with myelofibrosis and a novel constitutional chromosomal translocation t(3;4)(q13;q12). Journal of Clinical Pathology, 49, 259-262.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.