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American Journal of Medical Genetics|December 31, 1997
Private multiple congenital anomaly syndromes may result from unbalanced subtle translocations: t(2q;4p) explains the Lambotte syndromeC Herens, M Jamar, M L Alvarez-Gonzalez, et al.European Journal of Human Genetics : EJHG|February 15, 2001
Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test?A Verloes, Y Gillerot, L Van Maldergem, et al.Revue Medicale De Liege|August 26, 1998
[Myelodysplastic syndromes: preleukemic syndromes]F Tassin, J P Hermanne, N Schaaf-Lafontaine, et al.Cancer Genetics and Cytogenetics|April 13, 1999
Translocation (2;3)(p21;q26) as the sole anomaly in a case of primary myelofibrosisC Herens, J P Hermanne, F Tassin, et al.British Journal of Haematology|August 10, 2000
Deletion of the 5'-ABL region: a recurrent anomaly detected by fluorescence in situ hybridization in about 10% of Philadelphia-positive chronic myeloid leukaemia patientsC Herens, F Tassin, V Lemaire, et al.Genes, Chromosomes & Cancer|August 5, 2000
MLL amplification in myeloid leukemias: A study of 14 cases with multiple copies of 11q23L Michaux, I Wlodarska, M Stul, et al.Leukemia|June 6, 2008
Acute myeloid leukaemia with 8p11 (MYST3) rearrangement: an integrated cytologic, cytogenetic and molecular study by the groupe francophone de cytogénétique hématologiqueC Gervais, A Murati, C Helias, et al.Leukemia|October 12, 2007
Hyperdiploid karyotypes in acute myeloid leukemia define a novel entity: a study of 38 patients from the Groupe Francophone de Cytogenetique Hematologique (GFCH)I Luquet, J L Laï, C Barin, et al.Leukemia|September 13, 2003
t(5;14)/HOX11L2-positive T-cell acute lymphoblastic leukemia. A collaborative study of the Groupe Français de Cytogénétique Hématologique (GFCH)R Berger, N Dastugue, M Busson, et al.Pageof 4