Search Results - "Hecht, B K"

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    Mapping FRA11A, a folate-sensitive fragile site in human chromosome band 11q13.3 by Perucca-Lostanlen, D, Hecht, B K, Courseaux, A, Grosgeorge, J, Hecht, F, Gaudray, P

    Published in Cytogenetics and cell genetics (01-01-1997)
    “…FRA11A, a rare folate-sensitive fragile site assigned to 11q13.3, lies in an area of genomic instability associated with several diseases and amplification…”
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    Lack of Involvement of the c-fms and N-myc Genes by Chromosomal Translocation t(2;5)(p23;q35) Common to Malignancies With Features of So-Called Malignant Histiocytosis by Morgan, Rodman, Smith, Stephen D., Hecht, Barbara K., Christy, Valerie, Mellentin, Julia D., Warnke, Roger, Cleary, Michael L.

    Published in Blood (01-06-1989)
    “…We report the molecular, cytogenetic, and immunologic characterization of three hematologic malignancies that contained characteristic t(2;5) chromosomal…”
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    Clinical and Biologic Characterization of T-Cell Neoplasias With Rearrangements of Chromosome 7 Band q34 by Smith, Stephen D., Morgan, Rodman, Gemmell, Robert, Amylon, Michael D., Link, Michael P., Linker, Charles, Hecht, Barbara K., Warnke, Roger, Glader, Bertil E., Hecht, Frederick

    Published in Blood (01-02-1988)
    “…In T cell malignancy, rearrangements of chromosome 14 have been observed with a break in the band that contains the a chain gene for the T cell receptor (TCR)…”
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    Direct molecular diagnosis of myotonic dystrophy by Hecht, B K, Donnelly, A, Gedeon, A K, Byard, R W, Haan, E A, Mulley, J C

    Published in Clinical genetics (01-06-1993)
    “…Myotonic dystrophy (DM) arises from an unstable trinucleotide (CTGn) repeat sequence within the DM locus at 19q13.3. Twenty-three myotonic dystrophy families…”
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    Y chromosome-specific DNA sequences in turner-syndrome mosaicism by GEMMILL, R. M, PEARCE-BIRGE, L, BIXENMAN, H, HECHT, B. K, ALLANSON, J. E

    Published in American journal of human genetics (01-08-1987)
    “…Phenotypic females with Y-chromosomal material in their genome have an increased risk for development of gonadal malignancy. The detection and identification…”
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    The Journal “Impact Factor”: A Misnamed, Misleading, Misused Measure by Hecht, Frederick, Hecht, Barbara K, Sandberg, Avery A

    Published in Cancer genetics and cytogenetics (15-07-1998)
    “…The Institute for Scientific Information (ISI), a database publishing company that publishes Current Contents and Science Citation Index, has devised and…”
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    Behavior in Klinefelter syndrome, or where there is smoke there may not be a fire by Hecht, F, Hecht, B K

    Published in Pediatrics (Evanston) (01-12-1990)
    “…In Reply.— Drs Hecht and Hecht smell smoke but see no fire. They also may not see the forest for the trees. When we became aware of four individuals with…”
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    BCL3 rearrangements and t(14;19) in chronic lymphocytic leukemia and other B-cell malignancies: A molecular and cytogenetic study by McKeithan, Timothy W., Takimoto, Glenn S., Ohno, Hitoshi, Bjorling, Vincent S., Morgan, Rodman, Hecht, Barbara K., Dubé, Ian, Sandberg, Avery A., Rowley, Janet D.

    Published in Genes chromosomes & cancer (01-09-1997)
    “…The t(14;19)(q32.3;q13.1) is a recurring translocation found in the neoplastic cells of some patients with chronic lymphocytic leukemia (CLL) or other…”
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    X;6 translocation in a child with congenital acute lymphocytic leukemia by Carney, L A, Kinney, J S, Higgins, R R, Freeman, A I, Hecht, B K, Woods, G M

    Published in Cancer (01-02-1992)
    “…A case of congenital acute lymphoblastic leukemia (ALL) displayed an X;6 translocation. This is the third reported case of ALL with an X;6 translocation. In…”
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    Risks with translocation in "typus edinburgensis" by Hecht, F, Hecht, B K

    Published in Pediatrics (Evanston) (01-02-1992)
    “…To the Editor.— In 1974 Habel1 described five infants in an Edinburgh family with dysmorphic facial features, developmental delay, and early demise. He called…”
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    Telomeric fusion in pre-T-cell acute lymphoblastic leukemia by MORGAN, R, JARZABEK, V, JAFFE, J. P, HECHT, B. K, SANDBERG, A. A

    Published in Human genetics (01-07-1986)
    “…Telomeric fusion, a rare phenomenon, was observed in malignant cells from the peripheral blood of an 18-year-old male with rapidly progressive pre-T-cell acute…”
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    Chromosome sublocalization of a cDNA for human DNA polymerase-beta to 8p11----p12 by Cannizzaro, L A, Bollum, F J, Huebner, K, Croce, C M, Cheung, L C, Xu, X, Hecht, B K, Hecht, F, Chang, L M

    Published in Cytogenetics and cell genetics (01-01-1988)
    “…We have localized a cDNA fragment that codes for human DNA polymerase-beta. Using somatic cell and in situ hybridization techniques, this cDNA was cloned by…”
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    Unexpected lambda chain expression in lymphocytic malignancy by Hecht, F, Morgan, R, Hecht, B K

    “…Specific chromosome changes occur in the initiation and progression of cancer. A translocation between chromosomes 14 and 18 arises as a primary cytogenetic…”
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    Cancer in ataxia-telangiectasia patients by Hecht, F, Hecht, B K

    Published in Cancer genetics and cytogenetics (01-05-1990)
    “…A gene locus for ataxia-telangiectasia (A-T) is in chromosome region 11q22 to 11q23 and predisposes to cancer. Ataxia-telangiectasia patients appear to have…”
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