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Results: 1-17 |
Results: 17

Authors: COSTA T LAMBERT M TESHIMA I RAY PN RICHER CL DALLAIRE L
Citation: T. Costa et al., MONOZYGOTIC TWINS WITH 45,X 46,XY MOSAICISM DISCORDANT FOR PHENOTYPICSEX/, American journal of medical genetics, 75(1), 1998, pp. 40-44

Authors: CHAKRABARTI S ZHANG XX RICHER CL
Citation: S. Chakrabarti et al., INFLUENCE OF DURATION OF EXPOSURE TO STYRENE OXIDE ON SISTER-CHROMATID EXCHANGES AND CELL-CYCLE KINETICS IN CULTURED HUMAN BLOOD-LYMPHOCYTES IN-VITRO, Mutation research. Genetic toxicology and environmental mutagenesis, 395(1), 1997, pp. 37-45

Authors: LEMIEUX N BOUTOUIL M FETNI R QU JY DALLAIRE L RICHER CL
Citation: N. Lemieux et al., INTERSTITIAL TELOMERIC SEQUENCES AND FRAGILE SITES - A DILEMMA, Human genetics, 101(2), 1997, pp. 252-253

Authors: FETNI R RICHER CL MALFOY B DUTRILLAUX B LEMIEUX N
Citation: R. Fetni et al., CYTOLOGIC CHARACTERIZATION OF 2 DISTINCT ALPHA-SATELLITE DNA DOMAINS ON HUMAN-CHROMOSOME-7, USING DOUBLE-LABELING HYBRIDIZATIONS IN FLUORESCENCE AND ELECTRON-MICROSCOPY ON A MELANOMA CELL-LINE, Cancer genetics and cytogenetics, 96(1), 1997, pp. 17-22

Authors: DROUIN R BOUTOUIL M FETNI R HOLMQUIST GP SCOTT P RICHER CL LEMIEUX N
Citation: R. Drouin et al., DNA-REPLICATION ASYNCHRONY BETWEEN THE PATERNAL AND MATERNAL ALLELES OF IMPRINTED GENES DOES NOT STRADDLE THE R G TRANSITION/, Chromosoma, 106(6), 1997, pp. 405-411

Authors: BOUTOUIL M FETNI R QU JH DALLAIRE L RICHER CL LEMIEUX N
Citation: M. Boutouil et al., FRAGILE SITE AND INTERSTITIAL TELOMERE REPEAT SEQUENCES AT THE FUSIONPOINT OF A DE-NOVO (Y-13) TRANSLOCATION, Human genetics, 98(3), 1996, pp. 323-327

Authors: FETNI R DROUIN R RICHER CL LEMIEUX N
Citation: R. Fetni et al., COMPLEMENTARY REPLICATION R-BAND AND G-BAND PATTERNS INDUCED BY CELL BLOCKING AT THE R-BAND G-BAND TRANSITION, A POSSIBLE REGULATORY CHECKPOINT WITHIN THE S-PHASE OF THE CELL-CYCLE/, Cytogenetics and cell genetics, 75(2-3), 1996, pp. 172-179

Authors: FETNI R KRABCHI K MESSIER PE RICHER CL LEMIEUX N
Citation: R. Fetni et al., CHARACTERIZATION BY FLUORESCENCE AND ELECTRON-MICROSCOPY IN-SITU HYBRIDIZATION OF A DOUBLE Y-ISOCHROMOSOME, American journal of medical genetics, 63(3), 1996, pp. 454-457

Authors: DROUIN R BOUTOUIL M FETNI R SCOTT P HOLMQUIST GP RICHER CL LEMIEUX N
Citation: R. Drouin et al., THE REPLICATION ASYNCHRONY BETWEEN THE PATERNAL AND MATERNAL ALLELES OF IMPRINTED GENES DOES NOT STRADDLE THE R G TRANSITION/, American journal of human genetics, 57(4), 1995, pp. 625-625

Authors: LEMIEUX N MALFOY B FETNI R MULERIS M VOGT N RICHER CL DUTRILLAUX B
Citation: N. Lemieux et al., IN-SITU HYBRIDIZATION APPROACH AT INFRAGENIC LEVEL ON METAPHASE CHROMOSOMES, Cytogenetics and cell genetics, 66(2), 1994, pp. 107-112

Authors: CHAKRABARTI S DUHR MA SENECALQUEVILLON M RICHER CL
Citation: S. Chakrabarti et al., DOSE-DEPENDENT GENOTOXIC EFFECTS OF STYRENE ON HUMAN BLOOD-LYMPHOCYTES AND THE RELATIONSHIP TO ITS OXIDATIVE AND METABOLIC EFFECTS, Environmental and molecular mutagenesis, 22(2), 1993, pp. 85-92

Authors: RICHER CL CHAKRABARTI S SENECALQUEVILLON M DUHR MA ZHANG XX TARDIF R
Citation: Cl. Richer et al., CYTOGENETIC EFFECTS OF LOW-LEVEL EXPOSURE TO TOLUENE, XYLENE, AND THEIR MIXTURE ON HUMAN BLOOD-LYMPHOCYTES, International archives of occupational and environmental health, 64(8), 1993, pp. 581-585

Authors: ZHANG XX CHAKRABARTI S MALICK MA RICHER CL
Citation: Xx. Zhang et al., CYTOGENOTOXICITY OF N-ACETYL-S-(1 2-PHENYL-2-HYDROXYETHYL)-CYSTEINE (NAPEC) IN CULTURED HUMAN BLOOD-LYMPHOCYTES/, MUTATION RESEARCH, 319(2), 1993, pp. 121-127

Authors: ZHANG XX CHAKRABARTI S MALICK AM RICHER CL
Citation: Xx. Zhang et al., EFFECTS OF DIFFERENT STYRENE METABOLITES ON CYTOTOXICITY, SISTER-CHROMATID EXCHANGES AND CELL-CYCLE KINETICS IN HUMAN WHOLE-BLOOD LYMPHOCYTES IN-VITRO, MUTATION RESEARCH, 302(4), 1993, pp. 213-218

Authors: LEMIEUX N FETNI R VOGT N MALFOY B MULERIS M DUTRILLAUX B RICHER CL
Citation: N. Lemieux et al., CHROMATIN COMPACTION AND CONDENSATION IN A REGION OF ALPHA-SATELLITE DNA AND WITHIN A GENE LOCUS - A FISH AND EMISH APPROACH, American journal of human genetics, 53(3), 1993, pp. 574-574

Authors: QU J MITCHELL G SINNETT D FETNI R LEMIEUX N RICHER CL DALLAIRE L
Citation: J. Qu et al., THE ANGELMAN SYNDROME (AS) AND PRADER-WILLI-SYNDROME (PWS) CRITICAL REGION - FAILURE TO DETECT A DELETION BY FISH USING MARKERS FOR 1R4-3R AND GABRB3 IN PATIENTS WITH CYTOGENETICALLY VISIBLE DELETIONS, American journal of human genetics, 53(3), 1993, pp. 591-591

Authors: TIHY F VOGT N MALFOY B RECAN D LETURCQ F KAPLAN JC COQUET M SERVILLE F GUILLARD JM DUTRILLAUX B RICHER CL LEMIEUX N
Citation: F. Tihy et al., PHENOTYPE DISCORDANCE BETWEEN A HEALTHY MOTHER AND HER DMD-AFFECTED DAUGHTER SHARING THE SAME MOLECULAR DELETION WITHIN THE DYSTROPHIN GENE- EVIDENCE SUPPORTING THE NONRANDOM X INACTIVATION, American journal of human genetics, 53(3), 1993, pp. 1762-1762
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