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Anticancer Research|May 7, 2013
VEGFR1 and NRP1 endothelial expressions predict distant relapse after radical prostatectomy in clinically localized prostate cancerMatthieu Talagas, Arnaud Uguen, Ronan Garlantezec, et al.
Acta Cytologica|November 28, 2013
Breast implant-associated anaplastic large-cell lymphoma can be a diagnostic challenge for pathologistsMatthieu Talagas, Arnaud Uguen, Françoise Charles-Petillon, et al.
Annales De Pathologie|September 27, 2012
[A silent-growing and fast-killing melanoma in a teenager]Arnaud Uguen, Matthieu Talagas, Isabelle Quintin-Roué, et al.
Journal of Biomedicine & Biotechnology|January 29, 2011
Using bacterial artificial chromosomes in leukemia research: the experience at the university cytogenetics laboratory in Brest, FranceEtienne De Braekeleer, Nathalie Douet-Guilbert, Audrey Basinko, et al.
Reproductive Biomedicine Online|June 4, 2009
Meiotic segregation of X-autosome translocation in two carriers and implications for assisted reproductionAurore Perrin, François Vialard, Nathalie Douet-Guilbert, et al.
Cancer Genetics and Cytogenetics|October 3, 2006
Deletion size characterization of der(9) deletions in Philadelphia-positive chronic myeloid leukemiaNathalie Douet-Guilbert, Frédéric Morel, Sylvia Quemener, et al.
Diagnostic Pathology|July 25, 2015
NRAS (Q61R), BRAF (V600E) immunohistochemistry: a concomitant tool for mutation screening in melanomasArnaud Uguen, Matthieu Talagas, Sebastian Costa, et al.
Annals of Hematology|March 20, 2008
Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and retained regionsNathalie Douet-Guilbert, Audrey Basinko, Frédéric Morel, et al.
Leukemia Research|July 16, 2003
t(4;11)(q21;p15), including one complex translocation t(1;4;11)(p32;q21;p15), in adult T-cell acute lymphoblastic leukemiaNathalie Douet-Guilbert, Frédéric Morel, Marie Josée Le Bris, et al.
Cancer Genetics and Cytogenetics|June 9, 2007
Evaluation of chromosome 5 aberrations in complex karyotypes of patients with myeloid disorders reveals their contribution to dicentric and tricentric chromosomes, resulting in the loss of critical 5q regionsAngèle Herry, Nathalie Douet-Guilbert, Frédéric Morel, et al.
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