Literature DB >> 7504523

In situ hybridization to interphase nuclei in acute leukemia.

S P Romana1, D Cherif, M Le Coniat, J Derré, M A Flexor, R Berger.   

Abstract

Numerical chromosome abnormalities were studied in 17 acute lymphoblastic leukemias and one hyperdiploid acute myeloblastic leukemia by fluorescence in situ hybridization (FISH) using YAC clones specific to chromosomes 21 and 6. The results agreed well with cytogenetic findings. Hyperdiploid leukemias with more than 50 chromosomes usually had 4 copies of chromosome 21 and three of chromosome 6, while diploid and pseudodiploid cases were confirmed to have two copies of the two chromosomes. Interesting discrepancies were also observed. In one patient, trisomy 6 was detected by FISH but not by cytogenetics because of the probable inclusion of a chromosome 6 segment within a marker chromosome. The percentages of nuclei with 3 or 4 spots (chromosome 21) and three spots (chromosome 6) in hyperdiploid cells were significantly different in some patients, whereas they might be identical from cytogenetic data.

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Year:  1993        PMID: 7504523     DOI: 10.1002/gcc.2870080206

Source DB:  PubMed          Journal:  Genes Chromosomes Cancer        ISSN: 1045-2257            Impact factor:   5.006


  5 in total

1.  Enrichment, immunomorphological, and genetic characterization of fetal cells circulating in maternal blood.

Authors:  Giovanna Vona; Christophe Béroud; Alexandra Benachi; Alice Quenette; Jean Paul Bonnefont; Serge Romana; Yves Dumez; Bernard Lacour; Patrizia Paterlini-Bréchot
Journal:  Am J Pathol       Date:  2002-01       Impact factor: 4.307

2.  Formation of Nup98-containing nuclear bodies in HeLa sublines is linked to genomic rearrangements affecting chromosome 11.

Authors:  Serge Romana; Isabelle Radford-Weiss; Jean-Michel Lapierre; Valérie Doye; Marie-Claude Geoffroy
Journal:  Chromosoma       Date:  2015-12-21       Impact factor: 4.316

3.  Involvement of a human gene related to the Drosophila spen gene in the recurrent t(1;22) translocation of acute megakaryocytic leukemia.

Authors:  T Mercher; M B Coniat; R Monni; M Mauchauffe; F Nguyen Khac; L Gressin; F Mugneret; T Leblanc; N Dastugue; R Berger; O A Bernard
Journal:  Proc Natl Acad Sci U S A       Date:  2001-05-08       Impact factor: 11.205

4.  Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition.

Authors:  Marlène Rio; Valérie Malan; Sarah Boissel; Annick Toutain; Ghislaine Royer; Stéphanie Gobin; Nicole Morichon-Delvallez; Catherine Turleau; Jean-Paul Bonnefont; Arnold Munnich; Michel Vekemans; Laurence Colleaux
Journal:  Eur J Hum Genet       Date:  2009-10-21       Impact factor: 4.246

5.  Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowth.

Authors:  Valérie Malan; Suzanne Chevallier; Gwendoline Soler; Christine Coubes; Didier Lacombe; Laurent Pasquier; Jean Soulier; Nicole Morichon-Delvallez; Catherine Turleau; Arnold Munnich; Serge Romana; Michel Vekemans; Valérie Cormier-Daire; Laurence Colleaux
Journal:  Eur J Hum Genet       Date:  2009-10-21       Impact factor: 4.246

  5 in total

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