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Cancer Genetics and Cytogenetics|November 1, 1990
Deletion of (7p13p14) in non-Hodgkin's lymphomaP Jonveaux, M Le Coniat, J Derré, et al.Leukemia|September 1, 1996
Isochromosome 7q and trisomy 8 are consistent primary, non-random chromosomal abnormalities associated with hepatosplenic T gamma/delta lymphomaP Jonveaux, M T Daniel, V Martel, et al.Genes, Chromosomes & Cancer|September 1, 1991
Cytogenetic studies in acute promyelocytic leukemia: a survey of secondary chromosomal abnormalitiesR Berger, M Le Coniat, J Derré, et al.Blood|November 14, 1997
AF6q21, a novel partner of the MLL gene in t(6;11)(q21;q23), defines a forkhead transcriptional factor subfamilyJ Hillion, M Le Coniat, P Jonveaux, et al.Cancer Genetics and Cytogenetics|March 1, 1996
t(1;19)(q23;p13) in a case of acute monocytic leukemiaH J Weh, P Jonveaux, D Seeger, et al.Human Genetics|February 24, 2001
A detailed analysis of the MECP2 gene: prevalence of recurrent mutations and gross DNA rearrangements in Rett syndrome patientsV Bourdon, C Philippe, O Labrune, et al.Journal of Human Genetics|August 11, 2006
Pure de-novo 5 Mb duplication at Xp11.22-p11.23 in a male: phenotypic and molecular characterizationC Bonnet, M J Grégoire, K Brochet, et al.American Journal of Medical Genetics. Part A|May 19, 2009
Aberrant GRIA3 transcripts with multi-exon duplications in a family with X-linked mental retardationC Bonnet, B Leheup, M Béri, et al.Journal of Human Genetics|July 25, 2008
Cryptic 7q21 and 9p23 deletions in a patient with apparently balanced de novo reciprocal translocation t(7;9)(q21;p23) associated with a dystonia-plus syndrome: paternal deletion of the epsilon-sarcoglycan (SGCE) geneC Bonnet, M-J Grégoire, M Vibert, et al.Pathologie-Biologie|May 16, 2006
[Microarray-based comparative genomic hybridization in the study of constitutional chromosomal abnormalities]M Béri-Dexheimer, C Bonnet, P Chambon, et al.Pageof 10