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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
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LOIGNON M
FETNI R
GORDON AJE
DROBETSKY EA
Citation: M. Loignon et al., A P53-INDEPENDENT PATHWAY FOR INDUCTION OF P21(WAF1CIP1) AND CONCOMITANT G(1) ARREST IN UV-IRRADIATED HUMAN SKIN FIBROBLASTS, Cancer research, 57(16), 1997, pp. 3390-3394
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
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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
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LEMIEUX N
MALFOY B
FETNI R
MULERIS M
VOGT N
RICHER CL
DUTRILLAUX B
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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
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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