about
Using bacterial artificial chromosomes in leukemia research: the experience at the university cytogenetics laboratory in Brest, FranceGenetic aspects of monomorphic teratozoospermia: a reviewCytogenetic studies in T-cell acute lymphoblastic leukemia (1981-2002).Meiotic segregation of translocations during male gametogenesis.Fluorescence in situ hybridization testing of chromosomes 6, 8, 9 and 11 in melanocytic tumors is difficult to automate and reveals tumor heterogeneity in melanomas.RUNX1 translocations and fusion genes in malignant hemopathies.RARA fusion genes in acute promyelocytic leukemia: a review.MLL partner genes in secondary acute lymphoblastic leukemia: report of a new partner PRRC1 and review of the literature.3q26/EVI1 rearrangements in myeloid hemopathies: a cytogenetic review.Geographic/ethnic variability of chromosomal and molecular abnormalities in leukemia.ROS1 fusions in cancer: a review.A study of aneuploidy and DNA fragmentation in spermatozoa of three men with sex chromosome mosaicism including a 45,X cell line.Inbreeding and kinship in Saguenay-Lac-St-Jean: a study of newborn samples 1956-1971.Identification of MLL partner genes in 27 patients with acute leukemia from a single cytogenetic laboratory.A p16-Ki-67-HMB45 immunohistochemistry scoring system as an ancillary diagnostic tool in the diagnosis of melanoma.Recurrent translocation (10;17)(p15;q21) in acute poorly differentiated myeloid leukemia likely results in ZMYND11-MBTD1 fusion.Prognostic impact of p15 gene aberrations in acute leukemia.Acute myeloid leukaemia (FAB AML-M4Eo) with cryptic insertion of cbfb resulting in cbfb-Myh11 fusion.A novel translocation (6;20)(q13;q12) in acute myeloid leukemia likely results in LMBRD1-CHD6 fusionGenealogy and geographical distribution of CFTR mutations in Saguenay Lac-Saint-Jean (Quebec, Canada)Autosomal recessive disorders in Saguenay-Lac-Saint-Jean (Quebec, Canada): estimation of inbreeding from isonymyA prevalence and fertility study of haemochromatosis in Saguenay-Lac-Saint-JeanGeographic distribution of 18 autosomal recessive disorders in the French Canadian population of Saguenay-Lac-Saint-Jean, QuebecGenetic epidemiology of sensorimotor polyneuropathy with or without agenesis of the corpus callosum in northeastern QuebecHomogénéité génétique des Canadiens français du Québec : mythe ou réalité?
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description
Belgisch arts (1950-2016)
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kanadischer Genetiker, Arzt, Genetiker und Arzt
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researcher ORCID ID = 0000-0002-5165-2207
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Marc De Braekeleer
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0000-0002-5165-2207
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1950-01-01T00:00:00Z
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2016-07-01T00:00:00Z
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