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Leukemia|December 1, 1994
Distinct MLL gene rearrangements associated with successive acute monocytic and lymphoblastic leukemias in the same patientP Jonveaux, J Hillion, O Bernard, et al.Journal of Medical Genetics|March 21, 1998
Characterisation of an inverted X chromosome (p11.2q21.3) associated with mental retardation using FISHF Sloan-Béna, C Philippe, B LeHeup, et al.Prenatal Diagnosis|March 10, 2001
Use of the Kleihauer test to detect fetal erythroblasts in the maternal circulationV Martel-Petit, C Petit, M Marchand, et al.European Journal of Medical Genetics|September 1, 2007
Prenatal diagnosis of mosaicism for 11q terminal deletionM Valduga, V Latger Cannard, C Philippe, et al.American Journal of Medical Genetics. Part A|February 3, 2004
Two cousins with partial trisomy 12q and monosomy 12p recombinants of a familial pericentric inversion of the chromosome 12Clotilde Lagier-Tourenne, E Ginglinger, Y Alembik, et al.Genes, Chromosomes & Cancer|January 1, 1990
Two distinct mechanisms for the SCL gene activation in the t(1;14) translocation of T-cell leukemiasO Bernard, P Guglielmi, P Jonveaux, et al.Annales De Biologie Clinique|June 14, 2003
[Acute myeloblastic leukemia without maturation (AML-M1) with basophilic elements and associated with translocation t(6;9)]S Dimicoli, A Fohlen-Walter, L Mansuy, et al.Blood|March 1, 1995
Aplastic anemia and paroxysmal nocturnal hemoglobinuria: search for a pathogenetic linkA Griscelli-Bennaceur, E Gluckman, M L Scrobohaci, et al.American Journal of Medical Genetics. Part A|May 17, 2007
Fortuitous FISH diagnosis of an interstitial microdeletion (5)(q31.1q31.2) in a girl suspected to present a cri-du-chat syndromeA L Mosca, P Callier, B Leheup, et al.Prenatal Diagnosis|February 16, 2010
A retrospective study by oligonucleotide array-CGH analysis in 50 fetuses with multiple malformationsM Valduga, C Philippe, P Bach Segura, et al.Pageof 10